ENST00000371712.4:c.1775G>A
MANE Select
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ENSP00000360777.3:p.Arg592Gln
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|
ENST00000676019.1:c.1673G>A
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ENSP00000501984.1:p.Arg558Gln
|
|
ENST00000371712.3:c.1775G>A
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ENSP00000360777.3:p.Arg592Gln
|
|
NM_019892.4:c.1775G>A
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NP_063945.2:p.Arg592Gln
|
|
XM_005266094.2:c.1772G>A
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XP_005266151.1:p.Arg591Gln
|
|
NM_001318502.1:c.1772G>A
|
NP_001305431.1:p.Arg591Gln
|
|
NM_019892.5:c.1775G>A
|
NP_063945.2:p.Arg592Gln
|
|
XM_017014926.1:c.1775G>A
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XP_016870415.1:p.Arg592Gln
|
|
XR_929828.2:n.2380G>A
|
|
|
NM_019892.6:c.1775G>A
MANE Select
|
NP_063945.2:p.Arg592Gln
|
|
NM_001318502.2:c.1772G>A
|
NP_001305431.1:p.Arg591Gln
|
|