ENST00000461574.2:c.4985T=
|
ENSP00000417241.2:p.Met1662=
|
|
ENST00000470026.6:c.4988T=
|
ENSP00000419274.2:p.Met1663=
|
|
ENST00000473961.6:c.4862T=
|
ENSP00000420201.2:p.Met1621=
|
|
ENST00000476777.6:c.4982T=
|
ENSP00000417554.2:p.Met1661=
|
|
ENST00000477152.6:c.4910T=
|
ENSP00000419988.2:p.Met1637=
|
|
ENST00000478531.6:c.1676T=
|
ENSP00000420412.2:p.Met559=
|
|
ENST00000489037.2:c.4910T=
|
ENSP00000420781.2:p.Met1637=
|
|
ENST00000493919.6:c.1538T=
|
ENSP00000418819.2:p.Met513=
|
|
ENST00000494123.6:c.4988T=
|
ENSP00000419103.2:p.Met1663=
|
|
ENST00000497488.2:c.4100T=
|
ENSP00000418986.2:p.Met1367=
|
|
ENST00000618469.2:c.4988T=
|
ENSP00000478114.2:p.Met1663=
|
|
ENST00000634433.2:c.4865T=
|
ENSP00000489431.2:p.Met1622=
|
|
ENST00000644379.2:c.5054T=
|
ENSP00000496570.2:p.Met1685=
|
|
ENST00000644555.2:c.1538T=
|
ENSP00000494614.2:p.Met513=
|
|
ENST00000652672.2:c.4847T=
|
ENSP00000498906.2:p.Met1616=
|
|
ENST00000484087.6:c.1550T=
|
ENSP00000419481.2:p.Met517=
|
|
ENST00000357654.9:c.4988T=
MANE Select
|
ENSP00000350283.3:p.Met1663=
|
|
ENST00000471181.7:c.5051T=
|
ENSP00000418960.2:p.Met1684=
|
|
ENST00000644379.1:c.1375T=
|
|
|
ENST00000352993.7:c.1562T=
|
ENSP00000312236.5:p.Met521=
|
|
ENST00000357654.7:c.4988T=
|
ENSP00000350283.3:p.Met1663=
|
|
ENST00000461221.5:c.*4771T=
|
ENSP00000418548.1:n.*4771T=
|
|
ENST00000468300.5:c.1676T=
|
ENSP00000417148.1:p.Met559=
|
|
ENST00000471181.6:c.5051T=
|
ENSP00000418960.2:p.Met1684=
|
|
ENST00000472490.1:n.141T=
|
|
|
ENST00000478531.5:c.1676T=
|
ENSP00000420412.1:p.Met559=
|
|
ENST00000484087.5:c.1301T=
|
ENSP00000419481.1:p.Met434=
|
|
ENST00000491747.6:c.1676T=
|
ENSP00000420705.2:p.Met559=
|
|
ENST00000493795.5:c.4847T=
|
ENSP00000418775.1:p.Met1616=
|
|
ENST00000493919.5:c.1538T=
|
ENSP00000418819.1:p.Met513=
|
|
ENST00000586385.5:c.5-3743T=
|
ENSP00000465818.1:n.5-3743T=
|
|
ENST00000591534.5:c.461T=
|
ENSP00000467329.1:p.Met154=
|
|
ENST00000591849.5:c.-98-17504T=
|
ENSP00000465347.1:n.-98-17504T=
|
|
NM_007294.3:c.4988T= , LRG_292t1:c.4988T=
|
NP_009225.1:p.Met1663=
|
|
NM_007297.3:c.4847T=
|
NP_009228.2:p.Met1616=
|
|
NM_007298.3:c.1676T=
|
NP_009229.2:p.Met559=
|
|
NM_007299.3:c.1676T=
|
NP_009230.2:p.Met559=
|
|
NM_007300.3:c.5051T=
|
NP_009231.2:p.Met1684=
|
|
NR_027676.1:n.5124T=
|
|
|
NM_007294.4:c.4988T=
MANE Select
|
NP_009225.1:p.Met1663=
|
|
NM_007297.4:c.4847T=
|
NP_009228.2:p.Met1616=
|
|
NM_007299.4:c.1676T=
|
NP_009230.2:p.Met559=
|
|
NM_007300.4:c.5051T=
|
NP_009231.2:p.Met1684=
|
|
NR_027676.2:n.5165T=
|
|
|