ENST00000696982.1:c.1117G>A
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ENSP00000513017.1:p.Ala373Thr
|
|
ENST00000527786.7:c.1096G>A
MANE Select
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ENSP00000433488.2:p.Ala366Thr
|
|
ENST00000281428.12:c.898G>A
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ENSP00000281428.8:p.Ala300Thr
|
|
ENST00000344954.10:c.517G>A
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ENSP00000339627.7:p.Ala173Thr
|
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ENST00000429175.7:c.*1018G>A
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ENSP00000399985.3:n.*1018G>A
|
|
ENST00000527786.6:c.1096G>A
|
ENSP00000433488.2:p.Ala366Thr
|
|
ENST00000528790.1:n.3679G>A
|
|
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ENST00000534087.3:c.997G>A
|
ENSP00000432950.1:p.Ala333Thr
|
|
ENST00000608303.5:c.*488G>A
|
ENSP00000477262.1:n.*488G>A
|
|
NM_001167681.2:c.997G>A
|
NP_001161153.1:p.Ala333Thr
|
|
NM_001271010.1:c.898G>A
|
NP_001257939.1:p.Ala300Thr
|
|
NM_001271012.1:c.517G>A
|
NP_001257941.1:p.Ala173Thr
|
|
NM_002017.4:c.1096G>A
|
NP_002008.2:p.Ala366Thr
|
|
XM_011542701.1:c.997G>A
|
XP_011541003.1:p.Ala333Thr
|
|
XM_011542702.1:c.970G>A
|
XP_011541004.1:p.Ala324Thr
|
|
XM_011542701.2:c.997G>A
|
XP_011541003.1:p.Ala333Thr
|
|
XM_017017405.1:c.997G>A
|
XP_016872894.1:p.Ala333Thr
|
|
XM_017017406.1:c.997G>A
|
XP_016872895.1:p.Ala333Thr
|
|
NM_002017.5:c.1096G>A
MANE Select
|
NP_002008.2:p.Ala366Thr
|
|
NM_001167681.3:c.997G>A
|
NP_001161153.1:p.Ala333Thr
|
|
NM_001271010.2:c.898G>A
|
NP_001257939.1:p.Ala300Thr
|
|
NM_001271012.2:c.517G>A
|
NP_001257941.1:p.Ala173Thr
|
|