ENST00000356392.9:c.1144G>T
MANE Select
|
ENSP00000348757.3:p.Gly382Cys
|
|
ENST00000356392.8:c.1144G>T
|
ENSP00000348757.3:p.Gly382Cys
|
|
ENST00000586836.5:c.571G>T
|
ENSP00000467429.1:p.Gly191Cys
|
|
ENST00000591179.5:c.964G>T
|
ENSP00000466800.1:p.Gly322Cys
|
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ENST00000591345.5:c.*1063G>T
|
ENSP00000467313.1:n.*1063G>T
|
|
NM_001302453.1:c.982G>T
|
NP_001289382.1:p.Gly328Cys
|
|
NM_001302454.1:c.964G>T
|
NP_001289383.1:p.Gly322Cys
|
|
NM_145045.4:c.1144G>T
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NP_659482.3:p.Gly382Cys
|
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XM_017026241.1:c.*38G>T
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XP_016881730.1:n.*38G>T
|
|
NM_145045.5:c.1144G>T
MANE Select
|
NP_659482.3:p.Gly382Cys
|
|
NM_001302454.2:c.964G>T
|
NP_001289383.1:p.Gly322Cys
|
|