ENST00000261937.11:c.4034A>C
MANE Select
|
ENSP00000261937.6:p.Glu1345Ala
|
|
ENST00000261937.10:c.4034A>C
|
ENSP00000261937.6:p.Glu1345Ala
|
|
ENST00000502603.5:n.734A>C
|
|
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NM_182925.4:c.4034A>C
|
NP_891555.2:p.Glu1345Ala
|
|
XM_011534477.1:c.4283A>C
|
XP_011532779.1:p.Glu1428Ala
|
|
XM_011534478.1:c.4265A>C
|
XP_011532780.1:p.Glu1422Ala
|
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XM_011534482.1:c.4052A>C
|
XP_011532784.1:p.Glu1351Ala
|
|
XM_011534483.1:c.3974A>C
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XP_011532785.1:p.Glu1325Ala
|
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XM_011534484.1:c.3575A>C
|
XP_011532786.1:p.Glu1192Ala
|
|
XR_941095.1:n.4320A>C
|
|
|
XM_011534478.3:c.4265A>C
|
XP_011532780.1:p.Glu1422Ala
|
|
XM_011534484.2:c.3575A>C
|
XP_011532786.1:p.Glu1192Ala
|
|
XM_017009263.1:c.*180A>C
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XP_016864752.1:n.*180A>C
|
|
XM_017009268.1:c.3956A>C
|
XP_016864757.1:p.Glu1319Ala
|
|
XR_001742050.2:n.4524A>C
|
|
|
NM_182925.5:c.4034A>C
MANE Select
|
NP_891555.2:p.Glu1345Ala
|
|