ENST00000643606.3:c.211A>T
MANE Select
|
ENSP00000494576.2:p.Ile71Phe
|
|
ENST00000644830.1:c.52A>T
|
ENSP00000495111.1:p.Ile18Phe
|
|
ENST00000651652.1:c.109A>T
|
ENSP00000498953.1:p.Ile37Phe
|
|
ENST00000326431.3:c.211A>T
|
ENSP00000324775.3:p.Ile71Phe
|
|
NM_147196.2:c.211A>T
|
NP_671729.2:p.Ile71Phe
|
|
XM_006713097.2:c.52A>T
|
XP_006713160.1:p.Ile18Phe
|
|
XM_011533574.1:c.52A>T
|
XP_011531876.1:p.Ile18Phe
|
|
XM_006713097.4:c.52A>T
|
XP_006713160.1:p.Ile18Phe
|
|
XM_024453446.1:c.52A>T
|
XP_024309214.1:p.Ile18Phe
|
|
NM_001370524.1:c.52A>T
|
NP_001357453.1:p.Ile18Phe
|
|
NM_001370525.1:c.52A>T
|
NP_001357454.1:p.Ile18Phe
|
|
NM_147196.3:c.211A>T
MANE Select
|
NP_671729.2:p.Ile71Phe
|
|