ENST00000328963.10:c.1087T=
MANE Select
|
ENSP00000330696.6:p.Cys363=
|
|
ENST00000261826.10:c.*540T=
|
ENSP00000261826.6:n.*540T=
|
|
ENST00000328963.9:c.1087T=
|
ENSP00000330696.6:p.Cys363=
|
|
ENST00000535250.5:c.1171T=
|
ENSP00000442572.2:n.1171T=
|
|
ENST00000535600.2:c.904T=
|
ENSP00000442470.1:n.904T=
|
|
ENST00000537312.5:c.*858T=
|
ENSP00000438586.1:n.*858T=
|
|
ENST00000538011.5:c.1226T=
|
ENSP00000439247.1:n.1226T=
|
|
ENST00000539606.5:c.1310T=
|
ENSP00000445325.1:n.1310T=
|
|
ENST00000539695.5:n.1256T=
|
|
|
ENST00000541022.5:c.877T=
|
ENSP00000441230.1:n.877T=
|
|
ENST00000541564.5:c.950T=
|
ENSP00000443640.1:n.950T=
|
|
ENST00000541716.5:c.1098T=
|
ENSP00000437729.1:n.1098T=
|
|
NM_002562.5:c.1087T=
|
NP_002553.3:p.Cys363=
|
|
NR_033948.1:n.1453T=
|
|
|
NR_033949.1:n.1369T=
|
|
|
NR_033950.1:n.1330T=
|
|
|
NR_033951.1:n.1314T=
|
|
|
NR_033952.1:n.1241T=
|
|
|
NR_033953.1:n.1154T=
|
|
|
NR_033954.1:n.1133T=
|
|
|
NR_033955.1:n.1093T=
|
|
|
NR_033956.1:n.1020T=
|
|
|
XM_011538418.1:c.820T=
|
XP_011536720.1:p.Cys274=
|
|
XM_011538419.1:c.775T=
|
XP_011536721.1:p.Cys259=
|
|
XM_011538420.1:c.220T=
|
XP_011536722.1:p.Cys74=
|
|
XR_945459.1:n.190-14928A=
|
|
|
XR_945460.1:n.299-14928A=
|
|
|
XM_011538419.3:c.775T=
|
XP_011536721.1:p.Cys259=
|
|
XM_011538420.3:c.220T=
|
XP_011536722.1:p.Cys74=
|
|
XM_017019364.2:c.727T=
|
XP_016874853.1:p.Cys243=
|
|
XM_017019365.2:c.727T=
|
XP_016874854.1:p.Cys243=
|
|
XM_017019366.2:c.334T=
|
XP_016874855.1:p.Cys112=
|
|
XM_017019367.2:c.334T=
|
XP_016874856.1:p.Cys112=
|
|
XR_001749352.2:n.186+26153A=
|
|
|
XR_001749353.2:n.304-14928A=
|
|
|
XR_001749354.2:n.186+26153A=
|
|
|
XR_945459.3:n.187-14928A=
|
|
|
XR_945460.3:n.299-14928A=
|
|
|
NM_002562.6:c.1087T=
MANE Select
|
NP_002553.3:p.Cys363=
|
|
NR_033948.2:n.1405T=
|
|
|
NR_033949.2:n.1321T=
|
|
|
NR_033950.2:n.1282T=
|
|
|
NR_033951.2:n.1266T=
|
|
|
NR_033952.2:n.1193T=
|
|
|
NR_033953.2:n.1097T=
|
|
|
NR_033954.2:n.1085T=
|
|
|
NR_033955.2:n.1045T=
|
|
|
NR_033956.2:n.972T=
|
|
|