ENST00000281928.9:c.3536T>G
MANE Select
|
ENSP00000281928.3:p.Phe1179Cys
|
|
ENST00000549786.2:c.2964T>G
|
|
|
ENST00000648379.1:n.1904T>G
|
|
|
ENST00000648737.1:n.3300T>G
|
|
|
ENST00000648825.1:n.276T>G
|
|
|
ENST00000648916.1:n.1547T>G
|
|
|
ENST00000649607.1:c.1720T>G
|
|
|
ENST00000649775.1:c.33T>G
|
|
|
ENST00000650226.1:c.3536T>G
|
ENSP00000496981.1:p.Phe1179Cys
|
|
ENST00000281928.7:c.3536T>G
|
ENSP00000281928.3:p.Phe1179Cys
|
|
NM_015335.4:c.3536T>G
|
NP_056150.1:p.Phe1179Cys
|
|
XM_011538080.1:c.3536T>G
|
XP_011536382.1:p.Phe1179Cys
|
|
XM_011538081.1:c.3533T>G
|
XP_011536383.1:p.Phe1178Cys
|
|
XM_011538082.1:c.3506T>G
|
XP_011536384.1:p.Phe1169Cys
|
|
XM_011538080.2:c.3536T>G
|
XP_011536382.1:p.Phe1179Cys
|
|
XM_011538081.2:c.3533T>G
|
XP_011536383.1:p.Phe1178Cys
|
|
XM_011538082.2:c.3506T>G
|
XP_011536384.1:p.Phe1169Cys
|
|
XM_017019090.1:c.3533T>G
|
XP_016874579.1:p.Phe1178Cys
|
|
NM_015335.5:c.3536T>G
MANE Select
|
NP_056150.1:p.Phe1179Cys
|
|