ENST00000420175.3:c.334T>C
MANE Select
|
ENSP00000391137.2:p.Tyr112His
|
|
ENST00000275838.5:c.334T>C
|
ENSP00000275838.1:p.Tyr112His
|
|
ENST00000377867.7:c.289T>C
|
ENSP00000367098.3:p.Tyr97His
|
|
ENST00000420175.2:c.334T>C
|
ENSP00000391137.2:p.Tyr112His
|
|
NM_001142459.1:c.334T>C
|
NP_001135931.2:p.Tyr112His
|
|
NM_001142460.1:c.334T>C
|
NP_001135932.2:p.Tyr112His
|
|
NM_080871.3:c.289T>C
|
NP_543147.2:p.Tyr97His
|
|
XM_005249949.3:c.469T>C
|
XP_005250006.1:p.Tyr157His
|
|
NM_001142459.2:c.334T>C
MANE Select
|
NP_001135931.2:p.Tyr112His
|
|
NM_080871.4:c.289T>C
|
NP_543147.2:p.Tyr97His
|
|