ENST00000578493.2:n.1122C>G
|
|
|
ENST00000699291.1:c.914C>G
|
ENSP00000514272.1:n.914C>G
|
|
ENST00000699292.1:n.1324C>G
|
|
|
ENST00000225275.4:c.1789C>G
MANE Select
|
ENSP00000225275.3:p.Pro597Ala
|
|
ENST00000225275.3:c.1789C>G
|
ENSP00000225275.3:p.Pro597Ala
|
|
ENST00000577220.1:c.183+64C>G
|
ENSP00000464668.1:n.183+64C>G
|
|
NM_000250.1:c.1789C>G , LRG_84t1:c.1789C>G
|
NP_000241.1:p.Pro597Ala
|
|
XM_011524821.1:c.1975C>G
|
XP_011523123.1:p.Pro659Ala
|
|
XM_011524822.1:c.1504C>G
|
XP_011523124.1:p.Pro502Ala
|
|
NM_000250.2:c.1789C>G
MANE Select
|
NP_000241.1:p.Pro597Ala
|
|