|
ENST00000578202.2:c.*1210C>T
(MYLK)
|
ENSP00000463691.2:n.*1210C>T
|
|
|
ENST00000685021.1:c.*960C>T
(MYLK)
|
ENSP00000508447.1:n.*960C>T
|
|
|
ENST00000685744.1:c.*960C>T
(MYLK)
|
ENSP00000510047.1:n.*960C>T
|
|
|
ENST00000685953.1:c.*960C>T
(MYLK)
|
ENSP00000510593.1:n.*960C>T
|
|
|
ENST00000686039.1:c.4089C>T
(MYLK)
|
|
|
|
ENST00000687434.1:c.*2921C>T
(MYLK)
|
ENSP00000509751.1:n.*2921C>T
|
|
|
ENST00000688024.1:c.*960C>T
(MYLK)
|
ENSP00000509803.1:n.*960C>T
|
|
|
ENST00000688223.1:c.*960C>T
(MYLK)
|
ENSP00000508935.1:n.*960C>T
|
|
|
ENST00000689868.1:n.6965C>T
(MYLK)
|
|
|
|
ENST00000691933.1:c.4329C>T
(MYLK)
|
|
|
|
ENST00000692507.1:n.2509C>T
(MYLK)
|
|
|
|
ENST00000693689.1:c.*960C>T
(MYLK)
|
ENSP00000510503.1:n.*960C>T
|
|
|
ENST00000360304.8:c.*960C>T
(MYLK)
MANE Select
|
ENSP00000353452.3:n.*960C>T
|
|
|
ENST00000354792.9:c.*960C>T
(MYLK)
|
ENSP00000346846.6:n.*960C>T
|
|
|
ENST00000359169.5:c.*960C>T
(MYLK)
|
ENSP00000352088.1:n.*960C>T
|
|
|
ENST00000360304.7:c.*960C>T
(MYLK)
|
ENSP00000353452.3:n.*960C>T
|
|
|
ENST00000360772.7:c.*960C>T
(MYLK)
|
ENSP00000354004.3:n.*960C>T
|
|
|
ENST00000418370.6:c.*960C>T
(MYLK)
|
ENSP00000428967.1:n.*960C>T
|
|
|
NM_053025.3:c.*960C>T
(MYLK)
|
NP_444253.3:n.*960C>T
|
|
|
NM_053026.3:c.*960C>T
(MYLK)
|
NP_444254.3:n.*960C>T
|
|
|
NM_053027.3:c.*960C>T
(MYLK)
|
NP_444255.3:n.*960C>T
|
|
|
NM_053028.3:c.*960C>T
(MYLK)
|
NP_444256.3:n.*960C>T
|
|
|
NM_053031.2:c.*960C>T
(MYLK)
|
NP_444259.1:n.*960C>T
|
|
|
NM_053032.2:c.*960C>T
(MYLK)
|
NP_444260.1:n.*960C>T
|
|
|
NR_038266.2:n.290-16349G>A
(MYLK-AS1)
|
|
|
|
NR_121654.1:n.197-16349G>A
(MYLK-AS1)
|
|
|
|
NM_001321309.1:c.*960C>T
(MYLK)
|
NP_001308238.1:n.*960C>T
|
|
|
NM_053031.3:c.*960C>T
(MYLK)
|
NP_444259.1:n.*960C>T
|
|
|
NM_053032.3:c.*960C>T
(MYLK)
|
NP_444260.1:n.*960C>T
|
|
|
XM_017006469.2:c.*960C>T
(MYLK)
|
XP_016861958.1:n.*960C>T
|
|
|
XM_017006470.2:c.*960C>T
(MYLK)
|
XP_016861959.1:n.*960C>T
|
|
|
XM_017006471.2:c.*960C>T
(MYLK)
|
XP_016861960.1:n.*960C>T
|
|
|
XM_017006472.2:c.*960C>T
(MYLK)
|
XP_016861961.1:n.*960C>T
|
|
|
XM_017006473.1:c.*960C>T
(MYLK)
|
XP_016861962.1:n.*960C>T
|
|
|
NM_001321309.2:c.*960C>T
(MYLK)
|
NP_001308238.1:n.*960C>T
|
|
|
NM_053025.4:c.*960C>T
(MYLK)
MANE Select
|
NP_444253.3:n.*960C>T
|
|
|
NM_053026.4:c.*960C>T
(MYLK)
|
NP_444254.3:n.*960C>T
|
|
|
NM_053027.4:c.*960C>T
(MYLK)
|
NP_444255.3:n.*960C>T
|
|
|
NM_053028.4:c.*960C>T
(MYLK)
|
NP_444256.3:n.*960C>T
|
|
|
NM_053031.4:c.*960C>T
(MYLK)
|
NP_444259.1:n.*960C>T
|
|
|
NM_053032.4:c.*960C>T
(MYLK)
|
NP_444260.1:n.*960C>T
|
|
