|
ENST00000346322.10:c.4755-2646C>T
(MYLK)
|
ENSP00000320622.6:n.4755-2646C>T
|
|
|
ENST00000508240.2:c.1401C>T
(MYLK)
|
ENSP00000422984.2:p.Asn467=
|
|
|
ENST00000684879.1:n.2633C>T
(MYLK)
|
|
|
|
ENST00000685021.1:c.2235C>T
(MYLK)
|
ENSP00000508447.1:p.Asn745=
|
|
|
ENST00000685170.1:n.214C>T
(MYLK)
|
|
|
|
ENST00000685259.1:c.2520C>T
(MYLK)
|
|
|
|
ENST00000685907.1:n.2782C>T
(MYLK)
|
|
|
|
ENST00000685953.1:c.1401C>T
(MYLK)
|
ENSP00000510593.1:p.Asn467=
|
|
|
ENST00000686039.1:c.2385C>T
(MYLK)
|
|
|
|
ENST00000686245.1:c.2118C>T
(MYLK)
|
ENSP00000509313.1:p.Asn706=
|
|
|
ENST00000686281.1:n.293C>T
(MYLK)
|
|
|
|
ENST00000686406.1:c.5001C>T
(MYLK)
|
ENSP00000509044.1:p.Asn1667=
|
|
|
ENST00000686458.1:n.1503C>T
(MYLK)
|
|
|
|
ENST00000686761.1:c.5001C>T
(MYLK)
|
ENSP00000508758.1:p.Asn1667=
|
|
|
ENST00000686822.1:n.4895C>T
(MYLK)
|
|
|
|
ENST00000687434.1:c.*1217C>T
(MYLK)
|
ENSP00000509751.1:n.*1217C>T
|
|
|
ENST00000687709.1:n.3056C>T
(MYLK)
|
|
|
|
ENST00000687848.1:c.5031C>T
(MYLK)
|
ENSP00000508761.1:p.Asn1677=
|
|
|
ENST00000688024.1:c.2235C>T
(MYLK)
|
ENSP00000509803.1:p.Asn745=
|
|
|
ENST00000688223.1:c.2031C>T
(MYLK)
|
ENSP00000508935.1:p.Asn677=
|
|
|
ENST00000689446.1:n.206C>T
(MYLK)
|
|
|
|
ENST00000689868.1:n.2729C>T
(MYLK)
|
|
|
|
ENST00000689918.1:n.1076C>T
(MYLK)
|
|
|
|
ENST00000690086.1:n.1102C>T
(MYLK)
|
|
|
|
ENST00000690167.1:n.2672C>T
(MYLK)
|
|
|
|
ENST00000690457.1:c.4239C>T
(MYLK)
|
ENSP00000508777.1:p.Asn1413=
|
|
|
ENST00000690534.1:n.1522C>T
(MYLK)
|
|
|
|
ENST00000691933.1:c.2625C>T
(MYLK)
|
|
|
|
ENST00000692811.1:n.451C>T
(MYLK)
|
|
|
|
ENST00000693689.1:c.4794C>T
(MYLK)
|
ENSP00000510503.1:p.Asn1598=
|
|
|
ENST00000360304.8:c.5001C>T
(MYLK)
MANE Select
|
ENSP00000353452.3:p.Asn1667=
|
|
|
ENST00000346322.9:c.4794C>T
(MYLK)
|
ENSP00000320622.5:p.Asn1598=
|
|
|
ENST00000354792.9:c.4794C>T
(MYLK)
|
ENSP00000346846.6:p.Asn1598=
|
|
|
ENST00000359169.5:c.4962-2646C>T
(MYLK)
|
ENSP00000352088.1:n.4962-2646C>T
|
|
|
ENST00000360304.7:c.5001C>T
(MYLK)
|
ENSP00000353452.3:p.Asn1667=
|
|
|
ENST00000360772.7:c.4962-2646C>T
(MYLK)
|
ENSP00000354004.3:n.4962-2646C>T
|
|
|
ENST00000464489.5:c.*4580C>T
(MYLK)
|
ENSP00000417798.1:n.*4580C>T
|
|
|
ENST00000475616.5:c.5001C>T
(MYLK)
|
ENSP00000418335.1:p.Asn1667=
|
|
|
NM_053025.3:c.5001C>T
(MYLK)
|
NP_444253.3:p.Asn1667=
|
|
|
NM_053026.3:c.4794C>T
(MYLK)
|
NP_444254.3:p.Asn1598=
|
|
|
NM_053027.3:c.4962-2646C>T
(MYLK)
|
NP_444255.3:n.4962-2646C>T
|
|
|
NM_053028.3:c.4755-2646C>T
(MYLK)
|
NP_444256.3:n.4755-2646C>T
|
|
|
NR_038266.2:n.383G>A
(MYLK-AS1)
|
|
|
|
NR_121654.1:n.290G>A
(MYLK-AS1)
|
|
|
|
XM_011512860.1:c.5001C>T
(MYLK)
|
XP_011511162.1:p.Asn1667=
|
|
|
XM_011512861.1:c.4797C>T
(MYLK)
|
XP_011511163.1:p.Asn1599=
|
|
|
XM_011512862.1:c.4473C>T
(MYLK)
|
XP_011511164.1:p.Asn1491=
|
|
|
NM_001321309.1:c.4473C>T
(MYLK)
|
NP_001308238.1:p.Asn1491=
|
|
|
XM_011512860.3:c.5031C>T
(MYLK)
|
XP_011511162.2:p.Asn1677=
|
|
|
XM_011512861.3:c.4827C>T
(MYLK)
|
XP_011511163.2:p.Asn1609=
|
|
|
XM_017006469.2:c.2235C>T
(MYLK)
|
XP_016861958.1:p.Asn745=
|
|
|
XM_017006470.2:c.1401C>T
(MYLK)
|
XP_016861959.1:p.Asn467=
|
|
|
XM_017006471.2:c.1401C>T
(MYLK)
|
XP_016861960.1:p.Asn467=
|
|
|
XM_024453532.1:c.5031C>T
(MYLK)
|
XP_024309300.1:p.Asn1677=
|
|
|
XM_024453533.1:c.5001C>T
(MYLK)
|
XP_024309301.1:p.Asn1667=
|
|
|
XM_024453534.1:c.4824C>T
(MYLK)
|
XP_024309302.1:p.Asn1608=
|
|
|
XM_024453535.1:c.4794C>T
(MYLK)
|
XP_024309303.1:p.Asn1598=
|
|
|
XM_024453536.1:c.5001C>T
(MYLK)
|
XP_024309304.1:p.Asn1667=
|
|
|
XM_024453537.1:c.5001C>T
(MYLK)
|
XP_024309305.1:p.Asn1667=
|
|
|
NM_001321309.2:c.4473C>T
(MYLK)
|
NP_001308238.1:p.Asn1491=
|
|
|
NM_053025.4:c.5001C>T
(MYLK)
MANE Select
|
NP_444253.3:p.Asn1667=
|
|
|
NM_053026.4:c.4794C>T
(MYLK)
|
NP_444254.3:p.Asn1598=
|
|
|
NM_053027.4:c.4962-2646C>T
(MYLK)
|
NP_444255.3:n.4962-2646C>T
|
|
|
NM_053028.4:c.4755-2646C>T
(MYLK)
|
NP_444256.3:n.4755-2646C>T
|
|
