ENST00000281928.9:c.2718T>G
MANE Select
|
ENSP00000281928.3:p.Val906=
|
|
ENST00000548743.2:c.2688T>G
|
ENSP00000448553.2:p.Val896=
|
|
ENST00000549786.2:c.2146T>G
|
|
|
ENST00000647927.1:n.3091T>G
|
|
|
ENST00000648173.1:n.1513T>G
|
|
|
ENST00000648379.1:n.1086T>G
|
|
|
ENST00000648737.1:n.2482T>G
|
|
|
ENST00000648916.1:n.729T>G
|
|
|
ENST00000649607.1:c.902T>G
|
|
|
ENST00000650226.1:c.2718T>G
|
ENSP00000496981.1:p.Val906=
|
|
ENST00000281928.7:c.2718T>G
|
ENSP00000281928.3:p.Val906=
|
|
NM_015335.4:c.2718T>G
|
NP_056150.1:p.Val906=
|
|
XM_011538080.1:c.2718T>G
|
XP_011536382.1:p.Val906=
|
|
XM_011538081.1:c.2715T>G
|
XP_011536383.1:p.Val905=
|
|
XM_011538082.1:c.2688T>G
|
XP_011536384.1:p.Val896=
|
|
XM_011538080.2:c.2718T>G
|
XP_011536382.1:p.Val906=
|
|
XM_011538081.2:c.2715T>G
|
XP_011536383.1:p.Val905=
|
|
XM_011538082.2:c.2688T>G
|
XP_011536384.1:p.Val896=
|
|
XM_017019090.1:c.2715T>G
|
XP_016874579.1:p.Val905=
|
|
NM_015335.5:c.2718T>G
MANE Select
|
NP_056150.1:p.Val906=
|
|