ENST00000336411.7:c.1494T>G
|
ENSP00000337915.3:p.Pro498=
|
|
ENST00000651162.1:n.836T>G
|
|
|
ENST00000651514.1:c.1401T>G
MANE Select
|
ENSP00000498939.1:p.Pro467=
|
|
ENST00000651783.1:c.942T>G
|
ENSP00000498924.1:p.Pro314=
|
|
ENST00000652018.1:c.1254T>G
|
ENSP00000498733.1:p.Pro418=
|
|
ENST00000336411.6:c.1401T>G
|
ENSP00000337915.2:p.Pro467=
|
|
ENST00000354593.6:c.951T>G
|
ENSP00000346607.2:p.Pro317=
|
|
NM_001202855.2:c.1398T>G
|
NP_001189784.1:p.Pro466=
|
|
NM_017460.5:c.1401T>G
|
NP_059488.2:p.Pro467=
|
|
XM_011515841.1:c.1494T>G
|
XP_011514143.1:p.Pro498=
|
|
XM_011515842.1:c.1491T>G
|
XP_011514144.1:p.Pro497=
|
|
NM_017460.6:c.1401T>G
MANE Select
|
NP_059488.2:p.Pro467=
|
|
NM_001202855.3:c.1398T>G
|
NP_001189784.1:p.Pro466=
|
|