ENST00000281928.9:c.3099T>G
MANE Select
|
ENSP00000281928.3:p.Ser1033Arg
|
|
ENST00000548743.2:c.3069T>G
|
ENSP00000448553.2:p.Ser1023Arg
|
|
ENST00000549786.2:c.2527T>G
|
|
|
ENST00000648173.1:n.1894T>G
|
|
|
ENST00000648379.1:n.1467T>G
|
|
|
ENST00000648737.1:n.2863T>G
|
|
|
ENST00000648916.1:n.1110T>G
|
|
|
ENST00000649607.1:c.1283T>G
|
|
|
ENST00000650226.1:c.3099T>G
|
ENSP00000496981.1:p.Ser1033Arg
|
|
ENST00000281928.7:c.3099T>G
|
ENSP00000281928.3:p.Ser1033Arg
|
|
NM_015335.4:c.3099T>G
|
NP_056150.1:p.Ser1033Arg
|
|
XM_011538080.1:c.3099T>G
|
XP_011536382.1:p.Ser1033Arg
|
|
XM_011538081.1:c.3096T>G
|
XP_011536383.1:p.Ser1032Arg
|
|
XM_011538082.1:c.3069T>G
|
XP_011536384.1:p.Ser1023Arg
|
|
XM_011538080.2:c.3099T>G
|
XP_011536382.1:p.Ser1033Arg
|
|
XM_011538081.2:c.3096T>G
|
XP_011536383.1:p.Ser1032Arg
|
|
XM_011538082.2:c.3069T>G
|
XP_011536384.1:p.Ser1023Arg
|
|
XM_017019090.1:c.3096T>G
|
XP_016874579.1:p.Ser1032Arg
|
|
NM_015335.5:c.3099T>G
MANE Select
|
NP_056150.1:p.Ser1033Arg
|
|