ENST00000526189.3:c.568C>G
|
ENSP00000488104.2:p.Pro190Ala
|
|
ENST00000533357.5:c.649C>G
MANE Select
|
ENSP00000432943.1:p.Pro217Ala
|
|
ENST00000672287.2:c.61C>G
|
ENSP00000499818.2:p.Pro21Ala
|
|
ENST00000672602.2:c.649C>G
|
ENSP00000500814.2:p.Pro217Ala
|
|
ENST00000674861.1:n.712C>G
|
|
|
ENST00000463290.5:c.649C>G
|
ENSP00000431538.1:p.Pro217Ala
|
|
ENST00000476410.1:n.239C>G
|
|
|
ENST00000488271.1:n.87C>G
|
|
|
ENST00000491222.5:c.61C>G
|
ENSP00000431441.1:p.Pro21Ala
|
|
ENST00000526189.2:c.312C>G
|
|
|
ENST00000533357.4:c.649C>G
|
ENSP00000432943.1:p.Pro217Ala
|
|
NM_000530.6:c.649C>G , LRG_256t1:c.649C>G
|
NP_000521.2:p.Pro217Ala
|
|
NM_000530.7:c.649C>G
|
NP_000521.2:p.Pro217Ala
|
|
NM_001315491.1:c.649C>G
|
NP_001302420.1:p.Pro217Ala
|
|
XM_017001321.2:c.675+134C>G
|
XP_016856810.1:n.675+134C>G
|
|
NM_000530.8:c.649C>G
MANE Select
|
NP_000521.2:p.Pro217Ala
|
|
NM_001315491.2:c.649C>G
|
NP_001302420.1:p.Pro217Ala
|
|