ENST00000247933.9:c.838G>A
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ENSP00000247933.4:p.Ala280Thr
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ENST00000514224.2:c.838G>A
MANE Select
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ENSP00000425081.2:p.Ala280Thr
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ENST00000652070.1:n.894G>A
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|
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ENST00000247933.8:c.838G>A
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ENSP00000247933.4:p.Ala280Thr
|
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ENST00000514192.5:c.655G>A
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ENSP00000423685.1:p.Ala219Thr
|
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ENST00000514224.1:c.442G>A
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ENSP00000425081.1:p.Ala148Thr
|
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ENST00000514698.5:n.838G>A
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|
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NM_000203.4:c.838G>A
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NP_000194.2:p.Ala280Thr
|
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NR_110313.1:n.926G>A
|
|
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XM_006713882.2:c.442G>A
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XP_006713945.1:p.Ala148Thr
|
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XM_011513459.1:c.797G>A
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XP_011511761.1:p.Arg266His
|
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XM_011513460.1:c.697G>A
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XP_011511762.1:p.Ala233Thr
|
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XM_011513461.1:c.631G>A
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XP_011511763.1:p.Ala211Thr
|
|
XM_011513462.1:c.550G>A
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XP_011511764.1:p.Ala184Thr
|
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XM_011513463.1:c.550G>A
|
XP_011511765.1:p.Ala184Thr
|
|
XR_924947.1:n.907G>A
|
|
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NM_000203.5:c.838G>A
MANE Select
|
NP_000194.2:p.Ala280Thr
|
|
NM_001363576.1:c.442G>A
|
NP_001350505.1:p.Ala148Thr
|
|
XM_011513461.2:c.631G>A
|
XP_011511763.1:p.Ala211Thr
|
|
XM_017008163.1:c.-123G>A
|
XP_016863652.1:n.-123G>A
|
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