ENST00000235521.5:c.884C>A
MANE Select
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ENSP00000235521.4:p.Ala295Glu
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ENST00000235521.4:c.884C>A
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ENSP00000235521.4:p.Ala295Glu
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|
ENST00000369426.9:c.*250C>A
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ENSP00000358434.5:n.*250C>A
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NM_015836.3:c.884C>A
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NP_056651.1:p.Ala295Glu
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NM_201263.2:c.*250C>A
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NP_957715.1:n.*250C>A
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XM_005270350.2:c.830C>A
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XP_005270407.1:p.Ala277Glu
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XM_006710283.1:c.602C>A
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XP_006710346.1:p.Ala201Glu
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XM_011540493.1:c.815C>A
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XP_011538795.1:p.Ala272Glu
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XM_011540494.1:c.815C>A
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XP_011538796.1:p.Ala272Glu
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XM_011540495.1:c.626C>A
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XP_011538797.1:p.Ala209Glu
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XM_005270350.3:c.830C>A
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XP_005270407.1:p.Ala277Glu
|
|
XM_011540494.2:c.815C>A
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XP_011538796.1:p.Ala272Glu
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|
XM_011540495.2:c.626C>A
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XP_011538797.1:p.Ala209Glu
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|
XM_017000038.1:c.827C>A
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XP_016855527.1:p.Ala276Glu
|
|
XM_017000039.1:c.815C>A
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XP_016855528.1:p.Ala272Glu
|
|
XM_017000040.1:c.713C>A
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XP_016855529.1:p.Ala238Glu
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|
XM_017000041.2:c.545C>A
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XP_016855530.1:p.Ala182Glu
|
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XM_017000042.1:c.*219C>A
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XP_016855531.1:n.*219C>A
|
|
XM_024449826.1:c.815C>A
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XP_024305594.1:p.Ala272Glu
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|
XM_024449860.1:c.602C>A
|
XP_024305628.1:p.Ala201Glu
|
|
XM_024449871.1:c.602C>A
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XP_024305639.1:p.Ala201Glu
|
|
NM_001378226.1:c.815C>A
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NP_001365155.1:p.Ala272Glu
|
|
NM_001378227.1:c.815C>A
|
NP_001365156.1:p.Ala272Glu
|
|
NM_001378228.1:c.713C>A
|
NP_001365157.1:p.Ala238Glu
|
|
NM_001378229.1:c.626C>A
|
NP_001365158.1:p.Ala209Glu
|
|
NM_001378230.1:c.602C>A
|
NP_001365159.1:p.Ala201Glu
|
|
NM_001378231.1:c.*219C>A
|
NP_001365160.1:n.*219C>A
|
|
NM_015836.4:c.884C>A
MANE Select
|
NP_056651.1:p.Ala295Glu
|
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