ENST00000367400.8:c.4013A>T
MANE Select
|
ENSP00000356370.3:p.Asp1338Val
|
|
ENST00000367399.6:c.3677A>T
|
ENSP00000356369.2:p.Asp1226Val
|
|
ENST00000367400.7:c.4013A>T
|
ENSP00000356370.3:p.Asp1338Val
|
|
ENST00000448952.1:c.247A>T
|
ENSP00000395407.1:n.247A>T
|
|
ENST00000484075.5:c.*124A>T
|
ENSP00000433932.1:n.*124A>T
|
|
ENST00000535699.5:c.3941A>T
|
ENSP00000438786.1:p.Asp1314Val
|
|
ENST00000538660.5:c.2405A>T
|
ENSP00000438091.1:p.Asp802Val
|
|
NM_001193640.1:c.3677A>T
|
NP_001180569.1:p.Asp1226Val
|
|
NM_001257965.1:c.3941A>T
|
NP_001244894.1:p.Asp1314Val
|
|
NM_001257966.1:c.2405A>T
|
NP_001244895.1:p.Asp802Val
|
|
NM_201253.2:c.4013A>T
|
NP_957705.1:p.Asp1338Val
|
|
NR_047563.1:n.4014A>T
|
|
|
NR_047564.1:n.4464A>T
|
|
|
XM_011509366.1:c.*118A>T
|
XP_011507668.1:n.*118A>T
|
|
XM_011509367.1:c.3886A>T
|
XP_011507669.1:p.Met1296Leu
|
|
XM_011509368.1:c.3431A>T
|
XP_011507670.1:p.Asp1144Val
|
|
XM_011509369.1:c.2456A>T
|
XP_011507671.1:p.Asp819Val
|
|
XM_011509369.2:c.2456A>T
|
XP_011507671.1:p.Asp819Val
|
|
XM_017000851.1:c.3170A>T
|
XP_016856340.1:p.Asp1057Val
|
|
XM_017000852.1:c.4148A>T
|
XP_016856341.1:p.Asp1383Val
|
|
NM_201253.3:c.4013A>T
MANE Select
|
NP_957705.1:p.Asp1338Val
|
|
NM_001193640.2:c.3677A>T
|
NP_001180569.1:p.Asp1226Val
|
|
NM_001257965.2:c.3941A>T
|
NP_001244894.1:p.Asp1314Val
|
|
NR_047563.2:n.3966A>T
|
|
|
NR_047564.2:n.4416A>T
|
|
|
NM_001257966.2:c.2405A>T
|
NP_001244895.1:p.Asp802Val
|
|