ENST00000281928.9:c.4359C>G
MANE Select
|
ENSP00000281928.3:p.His1453Gln
|
|
ENST00000549786.2:c.3787C>G
|
|
|
ENST00000648379.1:n.2727C>G
|
|
|
ENST00000648737.1:n.4123C>G
|
|
|
ENST00000648825.1:n.1099C>G
|
|
|
ENST00000648916.1:n.2370C>G
|
|
|
ENST00000649146.1:n.1089C>G
|
|
|
ENST00000649607.1:c.2543C>G
|
|
|
ENST00000649775.1:c.856C>G
|
|
|
ENST00000650091.1:n.2335C>G
|
|
|
ENST00000650226.1:c.4359C>G
|
ENSP00000496981.1:p.His1453Gln
|
|
ENST00000281928.7:c.4359C>G
|
ENSP00000281928.3:p.His1453Gln
|
|
NM_015335.4:c.4359C>G
|
NP_056150.1:p.His1453Gln
|
|
XM_011538080.1:c.4359C>G
|
XP_011536382.1:p.His1453Gln
|
|
XM_011538081.1:c.4356C>G
|
XP_011536383.1:p.His1452Gln
|
|
XM_011538082.1:c.4329C>G
|
XP_011536384.1:p.His1443Gln
|
|
XM_011538080.2:c.4359C>G
|
XP_011536382.1:p.His1453Gln
|
|
XM_011538081.2:c.4356C>G
|
XP_011536383.1:p.His1452Gln
|
|
XM_011538082.2:c.4329C>G
|
XP_011536384.1:p.His1443Gln
|
|
XM_017019090.1:c.4356C>G
|
XP_016874579.1:p.His1452Gln
|
|
NM_015335.5:c.4359C>G
MANE Select
|
NP_056150.1:p.His1453Gln
|
|