ENST00000682275.1:c.1591G>A
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ENSP00000507852.1:p.Ala531Thr
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ENST00000683395.1:c.1532G>A
|
|
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ENST00000684087.1:c.1555G>A
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ENSP00000506978.1:p.Ala519Thr
|
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ENST00000506362.2:c.1306G>A
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ENSP00000424103.2:p.Ala436Thr
|
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ENST00000673642.1:c.1214G>A
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ENSP00000501242.1:p.Gly405Asp
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ENST00000673991.1:c.1591G>A
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ENSP00000501033.1:p.Ala531Thr
|
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ENST00000226760.5:c.1555G>A
MANE Select
|
ENSP00000226760.1:p.Ala519Thr
|
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ENST00000503569.5:c.1555G>A
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ENSP00000423337.1:p.Ala519Thr
|
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ENST00000507765.1:n.1740G>A
|
|
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NM_001145853.1:c.1555G>A
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NP_001139325.1:p.Ala519Thr
|
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NM_006005.3:c.1555G>A
MANE Select
|
NP_005996.2:p.Ala519Thr
|
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XM_017008586.1:c.1564G>A
|
XP_016864075.1:p.Ala522Thr
|
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