ENST00000367400.8:c.4175A>G
MANE Select
|
ENSP00000356370.3:p.Glu1392Gly
|
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ENST00000367399.6:c.3839A>G
|
ENSP00000356369.2:p.Glu1280Gly
|
|
ENST00000367400.7:c.4175A>G
|
ENSP00000356370.3:p.Glu1392Gly
|
|
ENST00000448952.1:c.409A>G
|
ENSP00000395407.1:n.409A>G
|
|
ENST00000484075.5:c.*286A>G
|
ENSP00000433932.1:n.*286A>G
|
|
ENST00000535699.5:c.4103A>G
|
ENSP00000438786.1:p.Glu1368Gly
|
|
ENST00000538660.5:c.2567A>G
|
ENSP00000438091.1:p.Glu856Gly
|
|
NM_001193640.1:c.3839A>G
|
NP_001180569.1:p.Glu1280Gly
|
|
NM_001257965.1:c.4103A>G
|
NP_001244894.1:p.Glu1368Gly
|
|
NM_001257966.1:c.2567A>G
|
NP_001244895.1:p.Glu856Gly
|
|
NM_201253.2:c.4175A>G
|
NP_957705.1:p.Glu1392Gly
|
|
NR_047563.1:n.4176A>G
|
|
|
NR_047564.1:n.4626A>G
|
|
|
XM_011509366.1:c.*280A>G
|
XP_011507668.1:n.*280A>G
|
|
XM_011509367.1:c.*154A>G
|
XP_011507669.1:n.*154A>G
|
|
XM_011509368.1:c.3593A>G
|
XP_011507670.1:p.Glu1198Gly
|
|
XM_011509369.1:c.2618A>G
|
XP_011507671.1:p.Glu873Gly
|
|
XM_011509369.2:c.2618A>G
|
XP_011507671.1:p.Glu873Gly
|
|
XM_017000851.1:c.3332A>G
|
XP_016856340.1:p.Glu1111Gly
|
|
XM_017000852.1:c.4310A>G
|
XP_016856341.1:p.Glu1437Gly
|
|
NM_201253.3:c.4175A>G
MANE Select
|
NP_957705.1:p.Glu1392Gly
|
|
NM_001193640.2:c.3839A>G
|
NP_001180569.1:p.Glu1280Gly
|
|
NM_001257965.2:c.4103A>G
|
NP_001244894.1:p.Glu1368Gly
|
|
NR_047563.2:n.4128A>G
|
|
|
NR_047564.2:n.4578A>G
|
|
|
NM_001257966.2:c.2567A>G
|
NP_001244895.1:p.Glu856Gly
|
|