ENST00000703783.1:n.203G>T
|
|
|
ENST00000703785.1:n.284G>T
|
|
|
ENST00000262464.9:c.3419G>T
MANE Select
|
ENSP00000262464.4:p.Cys1140Phe
|
|
ENST00000262464.8:c.3419G>T
|
ENSP00000262464.4:p.Cys1140Phe
|
|
ENST00000507835.5:c.-32G>T
|
ENSP00000426839.1:n.-32G>T
|
|
ENST00000508053.5:c.3419G>T
|
ENSP00000424571.1:p.Cys1140Phe
|
|
ENST00000508989.5:c.3320G>T
|
ENSP00000425596.1:p.Cys1107Phe
|
|
ENST00000619499.4:c.3416G>T
|
ENSP00000482132.1:p.Cys1139Phe
|
|
NM_001999.3:c.3419G>T
|
NP_001990.2:p.Cys1140Phe
|
|
XM_017009228.2:c.3266G>T
|
XP_016864717.1:p.Cys1089Phe
|
|
NM_001999.4:c.3419G>T
MANE Select
|
NP_001990.2:p.Cys1140Phe
|
|