ENST00000281928.9:c.3333T>G
MANE Select
|
ENSP00000281928.3:p.Val1111=
|
|
ENST00000549786.2:c.2761T>G
|
|
|
ENST00000648379.1:n.1701T>G
|
|
|
ENST00000648737.1:n.3097T>G
|
|
|
ENST00000648825.1:n.73T>G
|
|
|
ENST00000648916.1:n.1344T>G
|
|
|
ENST00000649607.1:c.1517T>G
|
|
|
ENST00000650226.1:c.3333T>G
|
ENSP00000496981.1:p.Val1111=
|
|
ENST00000281928.7:c.3333T>G
|
ENSP00000281928.3:p.Val1111=
|
|
NM_015335.4:c.3333T>G
|
NP_056150.1:p.Val1111=
|
|
XM_011538080.1:c.3333T>G
|
XP_011536382.1:p.Val1111=
|
|
XM_011538081.1:c.3330T>G
|
XP_011536383.1:p.Val1110=
|
|
XM_011538082.1:c.3303T>G
|
XP_011536384.1:p.Val1101=
|
|
XM_011538080.2:c.3333T>G
|
XP_011536382.1:p.Val1111=
|
|
XM_011538081.2:c.3330T>G
|
XP_011536383.1:p.Val1110=
|
|
XM_011538082.2:c.3303T>G
|
XP_011536384.1:p.Val1101=
|
|
XM_017019090.1:c.3330T>G
|
XP_016874579.1:p.Val1110=
|
|
NM_015335.5:c.3333T>G
MANE Select
|
NP_056150.1:p.Val1111=
|
|