ENST00000255531.8:c.2659G=
|
ENSP00000255531.7:p.Val887=
|
|
ENST00000373034.8:c.2800G=
MANE Select
|
ENSP00000362125.4:p.Val934=
|
|
ENST00000420881.6:c.2656G=
|
ENSP00000400327.2:p.Val886=
|
|
NM_001105243.1:c.2659G=
|
NP_001098713.1:p.Val887=
|
|
NM_001184880.1:c.2800G=
|
NP_001171809.1:p.Val934=
|
|
NM_020766.2:c.2656G=
|
NP_065817.2:p.Val886=
|
|
XM_011530997.1:c.2797G=
|
XP_011529299.1:p.Val933=
|
|
XM_011530997.2:c.2797G=
|
XP_011529299.1:p.Val933=
|
|
NM_001105243.2:c.2659G=
|
NP_001098713.1:p.Val887=
|
|
NM_001184880.2:c.2800G=
MANE Select
|
NP_001171809.1:p.Val934=
|
|
NM_020766.3:c.2656G=
|
NP_065817.2:p.Val886=
|
|