ENST00000270301.12:c.4148G>C
|
ENSP00000270301.6:p.Gly1383Ala
|
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ENST00000401500.7:c.4163G>C
MANE Select
|
ENSP00000384792.1:p.Gly1388Ala
|
|
ENST00000587391.6:c.*4023G>C
|
ENSP00000465525.1:n.*4023G>C
|
|
ENST00000679357.1:c.2243G>C
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|
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ENST00000679598.1:c.919-11G>C
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|
|
ENST00000679682.1:c.4148G>C
|
ENSP00000506226.1:p.Gly1383Ala
|
|
ENST00000679714.1:c.4157G>C
|
ENSP00000506627.1:p.Gly1386Ala
|
|
ENST00000679757.1:c.3812G>C
|
ENSP00000505158.1:p.Gly1271Ala
|
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ENST00000679858.1:c.*3545G>C
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ENSP00000505655.1:n.*3545G>C
|
|
ENST00000680211.1:c.764G>C
|
ENSP00000506102.1:p.Gly255Ala
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ENST00000680280.1:n.1666G>C
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|
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ENST00000680349.1:n.2812G>C
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|
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ENST00000680403.1:c.4148G>C
|
ENSP00000505677.1:p.Gly1383Ala
|
|
ENST00000680564.1:c.3914G>C
|
ENSP00000505582.1:p.Gly1305Ala
|
|
ENST00000680590.1:c.*2543G>C
|
ENSP00000505350.1:n.*2543G>C
|
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ENST00000680597.1:c.896G>C
|
|
|
ENST00000680739.1:c.1178G>C
|
|
|
ENST00000680773.1:n.2664G>C
|
|
|
ENST00000680806.1:c.*3466G>C
|
ENSP00000506418.1:n.*3466G>C
|
|
ENST00000680997.1:n.2095G>C
|
|
|
ENST00000681608.1:n.2008G>C
|
|
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ENST00000681625.1:c.*1495G>C
|
ENSP00000505555.1:n.*1495G>C
|
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ENST00000681648.1:n.2214G>C
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|
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ENST00000270301.11:c.4148G>C
|
ENSP00000270301.6:p.Gly1383Ala
|
|
ENST00000401500.6:c.4163G>C
|
ENSP00000384792.1:p.Gly1388Ala
|
|
ENST00000587391.5:c.*4023G>C
|
ENSP00000465525.1:n.*4023G>C
|
|
NM_001083961.1:c.4163G>C
|
NP_001077430.1:p.Gly1388Ala
|
|
NM_173636.4:c.4148G>C
|
NP_775907.4:p.Gly1383Ala
|
|
XM_005258809.2:c.4052G>C
|
XP_005258866.1:p.Gly1351Ala
|
|
XM_011526837.1:c.4148G>C
|
XP_011525139.1:p.Gly1383Ala
|
|
XM_011526838.1:c.3914G>C
|
XP_011525140.1:p.Gly1305Ala
|
|
XM_011526839.1:c.3812G>C
|
XP_011525141.1:p.Gly1271Ala
|
|
XM_011526840.1:c.3155G>C
|
XP_011525142.1:p.Gly1052Ala
|
|
XM_011526841.1:c.2741G>C
|
XP_011525143.1:p.Gly914Ala
|
|
XM_011526842.1:c.2594G>C
|
XP_011525144.1:p.Gly865Ala
|
|
XM_011526843.1:c.1910G>C
|
XP_011525145.1:p.Gly637Ala
|
|
XM_011526844.1:c.1910G>C
|
XP_011525146.1:p.Gly637Ala
|
|
XM_011526840.2:c.3155G>C
|
XP_011525142.1:p.Gly1052Ala
|
|
XM_011526841.2:c.2741G>C
|
XP_011525143.1:p.Gly914Ala
|
|
XM_011526844.2:c.1910G>C
|
XP_011525146.1:p.Gly637Ala
|
|
XM_017026665.1:c.4163G>C
|
XP_016882154.1:p.Gly1388Ala
|
|
NM_001083961.2:c.4163G>C
MANE Select
|
NP_001077430.1:p.Gly1388Ala
|
|
NM_173636.5:c.4148G>C
|
NP_775907.4:p.Gly1383Ala
|
|