ENST00000463045.3:c.292C>G
|
ENSP00000481376.2:p.Pro98Ala
|
|
ENST00000491274.6:c.421C>G
|
ENSP00000480482.2:p.Pro141Ala
|
|
ENST00000375499.8:c.463C>G
MANE Select
|
ENSP00000364649.3:p.Pro155Ala
|
|
ENST00000375499.7:c.463C>G
|
ENSP00000364649.3:p.Pro155Ala
|
|
ENST00000463045.2:c.292C>G
|
ENSP00000481376.1:p.Pro98Ala
|
|
ENST00000475506.1:n.380C>G
|
|
|
ENST00000485515.5:n.397C>G
|
|
|
ENST00000491274.5:c.421C>G
|
ENSP00000480482.1:p.Pro141Ala
|
|
NM_003000.2:c.463C>G , LRG_316t1:c.463C>G
|
NP_002991.2:p.Pro155Ala
|
|
NM_003000.3:c.463C>G
MANE Select
|
NP_002991.2:p.Pro155Ala
|
|