ENST00000336411.7:c.1447A=
|
ENSP00000337915.3:p.Met483=
|
|
ENST00000651162.1:n.789A=
|
|
|
ENST00000651514.1:c.1354A=
MANE Select
|
ENSP00000498939.1:p.Met452=
|
|
ENST00000651783.1:c.895A=
|
ENSP00000498924.1:p.Met299=
|
|
ENST00000652018.1:c.1207A=
|
ENSP00000498733.1:p.Met403=
|
|
ENST00000336411.6:c.1354A=
|
ENSP00000337915.2:p.Met452=
|
|
ENST00000354593.6:c.904A=
|
ENSP00000346607.2:p.Met302=
|
|
NM_001202855.2:c.1351A=
|
NP_001189784.1:p.Met451=
|
|
NM_017460.5:c.1354A=
|
NP_059488.2:p.Met452=
|
|
XM_011515841.1:c.1447A=
|
XP_011514143.1:p.Met483=
|
|
XM_011515842.1:c.1444A=
|
XP_011514144.1:p.Met482=
|
|
NM_017460.6:c.1354A=
MANE Select
|
NP_059488.2:p.Met452=
|
|
NM_001202855.3:c.1351A=
|
NP_001189784.1:p.Met451=
|
|