ENST00000336411.7:c.1380T=
|
ENSP00000337915.3:p.Pro460=
|
|
ENST00000651162.1:n.722T=
|
|
|
ENST00000651514.1:c.1287T=
MANE Select
|
ENSP00000498939.1:p.Pro429=
|
|
ENST00000651783.1:c.828T=
|
ENSP00000498924.1:p.Pro276=
|
|
ENST00000652018.1:c.1140T=
|
ENSP00000498733.1:p.Pro380=
|
|
ENST00000336411.6:c.1287T=
|
ENSP00000337915.2:p.Pro429=
|
|
ENST00000354593.6:c.837T=
|
ENSP00000346607.2:p.Pro279=
|
|
NM_001202855.2:c.1284T=
|
NP_001189784.1:p.Pro428=
|
|
NM_017460.5:c.1287T=
|
NP_059488.2:p.Pro429=
|
|
XM_011515841.1:c.1380T=
|
XP_011514143.1:p.Pro460=
|
|
XM_011515842.1:c.1377T=
|
XP_011514144.1:p.Pro459=
|
|
NM_017460.6:c.1287T=
MANE Select
|
NP_059488.2:p.Pro429=
|
|
NM_001202855.3:c.1284T=
|
NP_001189784.1:p.Pro428=
|
|