ENST00000328300.11:c.4938C>G
MANE Select
|
ENSP00000331902.7:p.Tyr1646Ter
|
|
ENST00000361603.7:c.4920C>G
|
ENSP00000354505.2:p.Tyr1640Ter
|
|
ENST00000510690.2:n.1432C>G
|
|
|
ENST00000644079.1:n.1769C>G
|
|
|
ENST00000328300.10:c.4938C>G
|
ENSP00000331902.6:p.Tyr1646Ter
|
|
ENST00000361603.6:c.4920C>G
|
ENSP00000354505.2:p.Tyr1640Ter
|
|
ENST00000504541.1:c.219+462C>G
|
ENSP00000424845.1:n.219+462C>G
|
|
ENST00000515658.1:c.325-914C>G
|
|
|
NM_000495.4:c.4920C>G
|
NP_000486.1:p.Tyr1640Ter
|
|
NM_033380.2:c.4938C>G
|
NP_203699.1:p.Tyr1646Ter
|
|
XM_005262070.2:c.4929C>G
|
XP_005262127.1:p.Tyr1643Ter
|
|
XM_006724616.2:c.4938C>G
|
XP_006724679.1:p.Tyr1646Ter
|
|
XM_011530849.1:c.4614C>G
|
XP_011529151.1:p.Tyr1538Ter
|
|
XM_011530851.1:c.2511C>G
|
XP_011529153.1:p.Tyr837Ter
|
|
XM_011530849.2:c.4953C>G
|
XP_011529151.2:p.Tyr1651Ter
|
|
XM_017029259.2:c.4944C>G
|
XP_016884748.1:p.Tyr1648Ter
|
|
XM_017029260.1:c.4935C>G
|
XP_016884749.1:p.Tyr1645Ter
|
|
XM_017029263.2:c.3273C>G
|
XP_016884752.1:p.Tyr1091Ter
|
|
NM_000495.5:c.4920C>G
|
NP_000486.1:p.Tyr1640Ter
|
|
NM_033380.3:c.4938C>G
MANE Select
|
NP_203699.1:p.Tyr1646Ter
|
|