|
ENST00000346322.10:c.5271T>C
(MYLK)
|
ENSP00000320622.6:p.Asp1757=
|
|
|
ENST00000508240.2:c.2031T>C
(MYLK)
|
ENSP00000422984.2:p.Asp677=
|
|
|
ENST00000578202.2:c.*136T>C
(MYLK)
|
ENSP00000463691.2:n.*136T>C
|
|
|
ENST00000583087.6:c.351T>C
(MYLK)
|
ENSP00000462118.1:p.Asp117=
|
|
|
ENST00000685021.1:c.2865T>C
(MYLK)
|
ENSP00000508447.1:p.Asp955=
|
|
|
ENST00000685170.1:n.844T>C
(MYLK)
|
|
|
|
ENST00000685259.1:c.3150T>C
(MYLK)
|
|
|
|
ENST00000685744.1:c.348T>C
(MYLK)
|
ENSP00000510047.1:p.Asp116=
|
|
|
ENST00000685907.1:n.3412T>C
(MYLK)
|
|
|
|
ENST00000685953.1:c.2028T>C
(MYLK)
|
ENSP00000510593.1:p.Asp676=
|
|
|
ENST00000686039.1:c.3015T>C
(MYLK)
|
|
|
|
ENST00000686245.1:c.2748T>C
(MYLK)
|
ENSP00000509313.1:p.Asp916=
|
|
|
ENST00000686281.1:n.923T>C
(MYLK)
|
|
|
|
ENST00000686406.1:c.5628T>C
(MYLK)
|
ENSP00000509044.1:p.Asp1876=
|
|
|
ENST00000686458.1:n.2133T>C
(MYLK)
|
|
|
|
ENST00000686761.1:c.5631T>C
(MYLK)
|
ENSP00000508758.1:p.Asp1877=
|
|
|
ENST00000687375.1:c.348T>C
(MYLK)
|
ENSP00000509867.1:p.Asp116=
|
|
|
ENST00000687434.1:c.*1847T>C
(MYLK)
|
ENSP00000509751.1:n.*1847T>C
|
|
|
ENST00000687709.1:n.3686T>C
(MYLK)
|
|
|
|
ENST00000687848.1:c.5661T>C
(MYLK)
|
ENSP00000508761.1:p.Asp1887=
|
|
|
ENST00000688024.1:c.2862T>C
(MYLK)
|
ENSP00000509803.1:p.Asp954=
|
|
|
ENST00000688223.1:c.2661T>C
(MYLK)
|
ENSP00000508935.1:p.Asp887=
|
|
|
ENST00000689446.1:n.833T>C
(MYLK)
|
|
|
|
ENST00000689868.1:n.5891T>C
(MYLK)
|
|
|
|
ENST00000689918.1:n.1706T>C
(MYLK)
|
|
|
|
ENST00000690167.1:n.3299T>C
(MYLK)
|
|
|
|
ENST00000690457.1:c.4869T>C
(MYLK)
|
ENSP00000508777.1:p.Asp1623=
|
|
|
ENST00000690656.1:n.336T>C
(MYLK)
|
|
|
|
ENST00000691367.1:n.327T>C
(MYLK)
|
|
|
|
ENST00000691933.1:c.3255T>C
(MYLK)
|
|
|
|
ENST00000692356.1:c.89-107T>C
(MYLK)
|
ENSP00000509805.1:n.89-107T>C
|
|
|
ENST00000692507.1:n.1435T>C
(MYLK)
|
|
|
|
ENST00000693689.1:c.5424T>C
(MYLK)
|
ENSP00000510503.1:p.Asp1808=
|
|
|
ENST00000360304.8:c.5631T>C
(MYLK)
MANE Select
|
ENSP00000353452.3:p.Asp1877=
|
|
|
ENST00000346322.9:c.5424T>C
(MYLK)
|
ENSP00000320622.5:p.Asp1808=
|
|
|
ENST00000354792.9:c.5424T>C
(MYLK)
|
ENSP00000346846.6:p.Asp1808=
|
|
|
ENST00000359169.5:c.5478T>C
(MYLK)
|
ENSP00000352088.1:p.Asp1826=
|
|
|
ENST00000360304.7:c.5631T>C
(MYLK)
|
ENSP00000353452.3:p.Asp1877=
|
|
|
ENST00000360772.7:c.5478T>C
(MYLK)
|
ENSP00000354004.3:p.Asp1826=
|
|
|
ENST00000418370.6:c.351T>C
(MYLK)
|
ENSP00000428967.1:p.Asp117=
|
|
|
ENST00000464489.5:c.*5210T>C
(MYLK)
|
ENSP00000417798.1:n.*5210T>C
|
|
|
ENST00000475616.5:c.5631T>C
(MYLK)
|
ENSP00000418335.1:p.Asp1877=
|
|
|
ENST00000578202.1:c.348T>C
(MYLK)
|
ENSP00000463691.1:p.Asp116=
|
|
|
ENST00000583087.5:c.351T>C
(MYLK)
|
ENSP00000462118.1:p.Asp117=
|
|
|
NM_053025.3:c.5631T>C
(MYLK)
|
NP_444253.3:p.Asp1877=
|
|
|
NM_053026.3:c.5424T>C
(MYLK)
|
NP_444254.3:p.Asp1808=
|
|
|
NM_053027.3:c.5478T>C
(MYLK)
|
NP_444255.3:p.Asp1826=
|
|
|
NM_053028.3:c.5271T>C
(MYLK)
|
NP_444256.3:p.Asp1757=
|
|
|
NM_053031.2:c.348T>C
(MYLK)
|
NP_444259.1:p.Asp116=
|
|
|
NM_053032.2:c.351T>C
(MYLK)
|
NP_444260.1:p.Asp117=
|
|
|
NR_038266.2:n.290-15275A>G
(MYLK-AS1)
|
|
|
|
NR_121654.1:n.197-15275A>G
(MYLK-AS1)
|
|
|
|
XM_011512860.1:c.5628T>C
(MYLK)
|
XP_011511162.1:p.Asp1876=
|
|
|
XM_011512861.1:c.5427T>C
(MYLK)
|
XP_011511163.1:p.Asp1809=
|
|
|
XM_011512862.1:c.5103T>C
(MYLK)
|
XP_011511164.1:p.Asp1701=
|
|
|
NM_001321309.1:c.5103T>C
(MYLK)
|
NP_001308238.1:p.Asp1701=
|
|
|
NM_053031.3:c.348T>C
(MYLK)
|
NP_444259.1:p.Asp116=
|
|
|
NM_053032.3:c.351T>C
(MYLK)
|
NP_444260.1:p.Asp117=
|
|
|
XM_011512860.3:c.5658T>C
(MYLK)
|
XP_011511162.2:p.Asp1886=
|
|
|
XM_011512861.3:c.5457T>C
(MYLK)
|
XP_011511163.2:p.Asp1819=
|
|
|
XM_017006469.2:c.2862T>C
(MYLK)
|
XP_016861958.1:p.Asp954=
|
|
|
XM_017006470.2:c.2028T>C
(MYLK)
|
XP_016861959.1:p.Asp676=
|
|
|
XM_017006471.2:c.2031T>C
(MYLK)
|
XP_016861960.1:p.Asp677=
|
|
|
XM_017006472.2:c.351T>C
(MYLK)
|
XP_016861961.1:p.Asp117=
|
|
|
XM_017006473.1:c.348T>C
(MYLK)
|
XP_016861962.1:p.Asp116=
|
|
|
XM_024453532.1:c.5661T>C
(MYLK)
|
XP_024309300.1:p.Asp1887=
|
|
|
XM_024453533.1:c.5631T>C
(MYLK)
|
XP_024309301.1:p.Asp1877=
|
|
|
XM_024453534.1:c.5454T>C
(MYLK)
|
XP_024309302.1:p.Asp1818=
|
|
|
XM_024453535.1:c.5424T>C
(MYLK)
|
XP_024309303.1:p.Asp1808=
|
|
|
XM_024453536.1:c.5631T>C
(MYLK)
|
XP_024309304.1:p.Asp1877=
|
|
|
XM_024453537.1:c.5631T>C
(MYLK)
|
XP_024309305.1:p.Asp1877=
|
|
|
NM_001321309.2:c.5103T>C
(MYLK)
|
NP_001308238.1:p.Asp1701=
|
|
|
NM_053025.4:c.5631T>C
(MYLK)
MANE Select
|
NP_444253.3:p.Asp1877=
|
|
|
NM_053026.4:c.5424T>C
(MYLK)
|
NP_444254.3:p.Asp1808=
|
|
|
NM_053027.4:c.5478T>C
(MYLK)
|
NP_444255.3:p.Asp1826=
|
|
|
NM_053028.4:c.5271T>C
(MYLK)
|
NP_444256.3:p.Asp1757=
|
|
|
NM_053031.4:c.348T>C
(MYLK)
|
NP_444259.1:p.Asp116=
|
|
|
NM_053032.4:c.351T>C
(MYLK)
|
NP_444260.1:p.Asp117=
|
|
