ENST00000281928.9:c.3002T>A
MANE Select
|
ENSP00000281928.3:p.Val1001Glu
|
|
ENST00000548743.2:c.2972T>A
|
ENSP00000448553.2:p.Val991Glu
|
|
ENST00000549786.2:c.2430T>A
|
|
|
ENST00000648173.1:n.1797T>A
|
|
|
ENST00000648379.1:n.1370T>A
|
|
|
ENST00000648737.1:n.2766T>A
|
|
|
ENST00000648916.1:n.1013T>A
|
|
|
ENST00000649607.1:c.1186T>A
|
|
|
ENST00000650226.1:c.3002T>A
|
ENSP00000496981.1:p.Val1001Glu
|
|
ENST00000281928.7:c.3002T>A
|
ENSP00000281928.3:p.Val1001Glu
|
|
NM_015335.4:c.3002T>A
|
NP_056150.1:p.Val1001Glu
|
|
XM_011538080.1:c.3002T>A
|
XP_011536382.1:p.Val1001Glu
|
|
XM_011538081.1:c.2999T>A
|
XP_011536383.1:p.Val1000Glu
|
|
XM_011538082.1:c.2972T>A
|
XP_011536384.1:p.Val991Glu
|
|
XM_011538080.2:c.3002T>A
|
XP_011536382.1:p.Val1001Glu
|
|
XM_011538081.2:c.2999T>A
|
XP_011536383.1:p.Val1000Glu
|
|
XM_011538082.2:c.2972T>A
|
XP_011536384.1:p.Val991Glu
|
|
XM_017019090.1:c.2999T>A
|
XP_016874579.1:p.Val1000Glu
|
|
NM_015335.5:c.3002T>A
MANE Select
|
NP_056150.1:p.Val1001Glu
|
|