ENST00000330062.8:c.664T>C
MANE Select
|
ENSP00000331897.4:p.Tyr222His
|
|
ENST00000330062.7:c.664T>C
|
ENSP00000331897.3:p.Tyr222His
|
|
ENST00000540499.2:c.508T>C
|
ENSP00000446147.2:p.Tyr170His
|
|
ENST00000559482.5:c.337T>C
|
ENSP00000453016.1:p.Tyr113His
|
|
ENST00000560061.1:c.*289T>C
|
ENSP00000453254.1:n.*289T>C
|
|
NM_001289910.1:c.508T>C , LRG_611t1:c.508T>C
|
NP_001276839.1:p.Tyr170His
|
|
NM_001290114.1:c.274T>C
|
NP_001277043.1:p.Tyr92His
|
|
NM_002168.3:c.664T>C , LRG_611t2:c.664T>C
|
NP_002159.2:p.Tyr222His
|
|
NM_001290114.2:c.274T>C
|
NP_001277043.1:p.Tyr92His
|
|
NM_002168.4:c.664T>C
MANE Select
|
NP_002159.2:p.Tyr222His
|
|