ENST00000319653.14:c.1757C>T
MANE Select
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ENSP00000318884.9:p.Ala586Val
|
|
ENST00000681210.1:c.56C>T
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ENSP00000505131.1:p.Ala19Val
|
|
ENST00000681741.1:c.56C>T
|
ENSP00000505116.1:p.Ala19Val
|
|
ENST00000681824.1:c.56C>T
|
ENSP00000505818.1:p.Ala19Val
|
|
ENST00000319653.13:c.1757C>T
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ENSP00000318884.9:p.Ala586Val
|
|
ENST00000447095.5:c.56C>T
|
ENSP00000409308.1:p.Ala19Val
|
|
NM_001305424.1:c.1757C>T
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NP_001292353.1:p.Ala586Val
|
|
NM_020066.4:c.1757C>T
|
NP_064450.3:p.Ala586Val
|
|
XM_011544237.1:c.1757C>T
|
XP_011542539.1:p.Ala586Val
|
|
XR_949151.1:n.1978C>T
|
|
|
NM_001348094.1:c.1757C>T
|
NP_001335023.1:p.Ala586Val
|
|
XM_011544237.3:c.1757C>T
|
XP_011542539.1:p.Ala586Val
|
|
XM_017001837.1:c.1757C>T
|
XP_016857326.1:p.Ala586Val
|
|
XM_017001838.1:c.1757C>T
|
XP_016857327.1:p.Ala586Val
|
|
NM_020066.5:c.1757C>T
MANE Select
|
NP_064450.3:p.Ala586Val
|
|
NM_001305424.2:c.1757C>T
|
NP_001292353.1:p.Ala586Val
|
|
NM_001348094.2:c.1757C>T
|
NP_001335023.1:p.Ala586Val
|
|