ENST00000440400.3:c.2617T>C
|
ENSP00000398393.2:p.Tyr873His
|
|
ENST00000697712.1:c.2491T>C
|
ENSP00000513410.1:p.Tyr831His
|
|
ENST00000252699.7:c.2632T>C
MANE Select
|
ENSP00000252699.2:p.Tyr878His
|
|
ENST00000424234.7:c.2632T>C
|
ENSP00000411187.4:p.Tyr878His
|
|
ENST00000440400.2:c.2617T>C
|
ENSP00000398393.2:p.Tyr873His
|
|
ENST00000252699.6:c.2632T>C
|
ENSP00000252699.2:p.Tyr878His
|
|
ENST00000390009.7:c.1975T>C
|
ENSP00000439497.1:p.Tyr659His
|
|
ENST00000424234.6:c.1462T>C
|
ENSP00000411187.3:p.Tyr488His
|
|
ENST00000440400.1:c.925T>C
|
ENSP00000398393.1:p.Tyr309His
|
|
ENST00000477174.1:n.451T>C
|
|
|
ENST00000497637.5:n.385T>C
|
|
|
ENST00000589528.1:c.286-661T>C
|
|
|
NM_004924.4:c.2632T>C
|
NP_004915.2:p.Tyr878His
|
|
XM_005259281.3:c.2617T>C
|
XP_005259338.1:p.Tyr873His
|
|
XM_005259282.3:c.2617T>C
|
XP_005259339.1:p.Tyr873His
|
|
XM_006723406.1:c.2632T>C
|
XP_006723469.1:p.Tyr878His
|
|
NM_001322033.1:c.2617T>C
|
NP_001308962.1:p.Tyr873His
|
|
NM_004924.5:c.2632T>C
|
NP_004915.2:p.Tyr878His
|
|
XM_005259281.5:c.2617T>C
|
XP_005259338.1:p.Tyr873His
|
|
XM_006723406.3:c.2632T>C
|
XP_006723469.1:p.Tyr878His
|
|
XM_017027331.2:c.2698T>C
|
XP_016882820.1:p.Tyr900His
|
|
NM_004924.6:c.2632T>C
MANE Select
|
NP_004915.2:p.Tyr878His
|
|
NM_001322033.2:c.2617T>C
|
NP_001308962.1:p.Tyr873His
|
|