ENST00000235521.5:c.883G>A
MANE Select
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ENSP00000235521.4:p.Ala295Thr
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|
ENST00000235521.4:c.883G>A
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ENSP00000235521.4:p.Ala295Thr
|
|
ENST00000369426.9:c.*249G>A
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ENSP00000358434.5:n.*249G>A
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NM_015836.3:c.883G>A
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NP_056651.1:p.Ala295Thr
|
|
NM_201263.2:c.*249G>A
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NP_957715.1:n.*249G>A
|
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XM_005270350.2:c.829G>A
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XP_005270407.1:p.Ala277Thr
|
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XM_006710283.1:c.601G>A
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XP_006710346.1:p.Ala201Thr
|
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XM_011540493.1:c.814G>A
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XP_011538795.1:p.Ala272Thr
|
|
XM_011540494.1:c.814G>A
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XP_011538796.1:p.Ala272Thr
|
|
XM_011540495.1:c.625G>A
|
XP_011538797.1:p.Ala209Thr
|
|
XM_005270350.3:c.829G>A
|
XP_005270407.1:p.Ala277Thr
|
|
XM_011540494.2:c.814G>A
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XP_011538796.1:p.Ala272Thr
|
|
XM_011540495.2:c.625G>A
|
XP_011538797.1:p.Ala209Thr
|
|
XM_017000038.1:c.826G>A
|
XP_016855527.1:p.Ala276Thr
|
|
XM_017000039.1:c.814G>A
|
XP_016855528.1:p.Ala272Thr
|
|
XM_017000040.1:c.712G>A
|
XP_016855529.1:p.Ala238Thr
|
|
XM_017000041.2:c.544G>A
|
XP_016855530.1:p.Ala182Thr
|
|
XM_017000042.1:c.*218G>A
|
XP_016855531.1:n.*218G>A
|
|
XM_024449826.1:c.814G>A
|
XP_024305594.1:p.Ala272Thr
|
|
XM_024449860.1:c.601G>A
|
XP_024305628.1:p.Ala201Thr
|
|
XM_024449871.1:c.601G>A
|
XP_024305639.1:p.Ala201Thr
|
|
NM_001378226.1:c.814G>A
|
NP_001365155.1:p.Ala272Thr
|
|
NM_001378227.1:c.814G>A
|
NP_001365156.1:p.Ala272Thr
|
|
NM_001378228.1:c.712G>A
|
NP_001365157.1:p.Ala238Thr
|
|
NM_001378229.1:c.625G>A
|
NP_001365158.1:p.Ala209Thr
|
|
NM_001378230.1:c.601G>A
|
NP_001365159.1:p.Ala201Thr
|
|
NM_001378231.1:c.*218G>A
|
NP_001365160.1:n.*218G>A
|
|
NM_015836.4:c.883G>A
MANE Select
|
NP_056651.1:p.Ala295Thr
|
|