ENST00000698508.1:c.1778T=
|
ENSP00000513759.1:p.Met593=
|
|
ENST00000698509.1:n.1918T=
|
|
|
ENST00000264972.10:c.1778T=
MANE Select
|
ENSP00000264972.5:p.Met593=
|
|
ENST00000264972.9:c.1778T=
|
ENSP00000264972.5:p.Met593=
|
|
ENST00000451498.2:c.857T=
|
ENSP00000400475.2:p.Met286=
|
|
ENST00000463643.5:n.1639T=
|
|
|
ENST00000487283.5:n.2830T=
|
|
|
NM_001079.3:c.1778T= , LRG_126t1:c.1778T=
|
NP_001070.2:p.Met593=
|
|
NM_207519.1:c.857T=
|
NP_997402.1:p.Met286=
|
|
XM_005264015.3:c.1760T=
|
XP_005264072.1:p.Met587=
|
|
XM_011511783.1:c.1736+1309T=
|
XP_011510085.1:n.1736+1309T=
|
|
XR_923018.1:n.1938+1309T=
|
|
|
XR_923019.1:n.1938+1309T=
|
|
|
XR_923020.1:n.2189T=
|
|
|
XM_017004867.1:c.2147T=
|
XP_016860356.1:p.Met716=
|
|
XM_017004868.1:c.2129T=
|
XP_016860357.1:p.Met710=
|
|
XM_017004869.1:c.2105+1309T=
|
XP_016860358.1:n.2105+1309T=
|
|
XR_001738925.1:n.3344+1309T=
|
|
|
XR_001738926.1:n.3344+1309T=
|
|
|
XR_001738927.1:n.3595T=
|
|
|
NM_001079.4:c.1778T=
MANE Select
|
NP_001070.2:p.Met593=
|
|
NM_001378594.1:c.1778T=
|
NP_001365523.1:p.Met593=
|
|
NM_207519.2:c.857T=
|
NP_997402.1:p.Met286=
|
|