ENST00000616995.5:n.1551T>G
|
|
|
ENST00000691517.1:n.1064T>G
|
|
|
ENST00000331968.11:c.1780T>G
MANE Select
|
ENSP00000333568.6:p.Phe594Val
|
|
ENST00000651571.1:c.1592T>G
|
ENSP00000498919.1:n.1592T>G
|
|
ENST00000651616.1:c.1661T>G
|
ENSP00000498661.1:n.1661T>G
|
|
ENST00000331968.9:c.1780T>G
|
ENSP00000333568.5:p.Phe594Val
|
|
ENST00000415220.6:c.1804T>G
|
ENSP00000390535.2:p.Phe602Val
|
|
ENST00000616995.4:c.1780T>G
|
ENSP00000482645.1:p.Phe594Val
|
|
NM_002742.2:c.1780T>G
|
NP_002733.2:p.Phe594Val
|
|
XM_005267859.1:c.1804T>G
|
XP_005267916.1:p.Phe602Val
|
|
XM_011536964.1:c.1576T>G
|
XP_011535266.1:p.Phe526Val
|
|
XM_011536965.1:c.1516T>G
|
XP_011535267.1:p.Phe506Val
|
|
XR_943493.1:n.1919T>G
|
|
|
NM_001330069.1:c.1804T>G
|
NP_001316998.1:p.Phe602Val
|
|
NM_001348390.1:c.1516T>G
|
NP_001335319.1:p.Phe506Val
|
|
XM_011536965.2:c.1516T>G
|
XP_011535267.1:p.Phe506Val
|
|
XM_017021462.1:c.1285T>G
|
XP_016876951.1:p.Phe429Val
|
|
XR_943493.2:n.2097T>G
|
|
|
NM_001330069.2:c.1804T>G
|
NP_001316998.1:p.Phe602Val
|
|
NM_002742.3:c.1780T>G
MANE Select
|
NP_002733.2:p.Phe594Val
|
|