ENST00000237596.7:c.1428T>G
MANE Select
|
ENSP00000237596.2:p.Cys476Trp
|
|
ENST00000237596.6:c.1428T>G
|
ENSP00000237596.2:p.Cys476Trp
|
|
ENST00000508588.5:c.-199+3293T>G
|
ENSP00000427131.1:n.-199+3293T>G
|
|
NM_000297.3:c.1428T>G
|
NP_000288.1:p.Cys476Trp
|
|
XM_011532028.1:c.1203T>G
|
XP_011530330.1:p.Cys401Trp
|
|
XM_011532029.1:c.708T>G
|
XP_011530331.1:p.Cys236Trp
|
|
XM_011532030.1:c.588T>G
|
XP_011530332.1:p.Cys196Trp
|
|
XR_244632.2:n.1523T>G
|
|
|
NR_156488.1:n.1515T>G
|
|
|
XM_011532028.2:c.1203T>G
|
XP_011530330.1:p.Cys401Trp
|
|
XM_011532030.2:c.588T>G
|
XP_011530332.1:p.Cys196Trp
|
|
NM_000297.4:c.1428T>G
MANE Select
|
NP_000288.1:p.Cys476Trp
|
|
NR_156488.2:n.1527T>G
|
|
|