ENST00000650793.2:n.513T>C
|
|
|
ENST00000697612.1:n.1191T>C
|
|
|
ENST00000374881.3:c.322T>C
|
ENSP00000364015.2:p.Tyr108His
|
|
ENST00000374882.8:c.334T>C
MANE Select
|
ENSP00000364016.4:p.Tyr112His
|
|
ENST00000650411.1:n.1655T>C
|
|
|
ENST00000650793.1:n.513T>C
|
|
|
ENST00000374881.2:c.322T>C
|
ENSP00000364015.2:p.Tyr108His
|
|
ENST00000374882.7:c.334T>C
|
ENSP00000364016.3:p.Tyr112His
|
|
ENST00000395339.7:c.296-34T>C
|
ENSP00000378748.3:n.296-34T>C
|
|
ENST00000484003.1:n.718T>C
|
|
|
NM_004159.4:c.322T>C
|
NP_004150.1:p.Tyr108His
|
|
NM_148919.3:c.334T>C
|
NP_683720.2:p.Tyr112His
|
|
NM_148919.4:c.334T>C
MANE Select
|
NP_683720.2:p.Tyr112His
|
|
NM_004159.5:c.322T>C
|
NP_004150.1:p.Tyr108His
|
|