ENST00000267845.8:c.1819G>T
MANE Select
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ENSP00000267845.3:p.Gly607Trp
|
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ENST00000267845.7:c.1819G>T
|
ENSP00000267845.3:p.Gly607Trp
|
|
ENST00000543581.5:c.1720G>T
|
ENSP00000440252.1:p.Gly574Trp
|
|
ENST00000559816.1:n.1563G>T
|
|
|
NM_001306146.1:c.1720G>T
|
NP_001293075.1:p.Gly574Trp
|
|
NM_002112.3:c.1819G>T
|
NP_002103.2:p.Gly607Trp
|
|
XM_011521479.1:c.1582G>T
|
XP_011519781.1:p.Gly528Trp
|
|
XM_011521480.1:c.1387G>T
|
XP_011519782.1:p.Gly463Trp
|
|
XM_017022094.1:c.1924G>T
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XP_016877583.1:p.Gly642Trp
|
|
XM_017022095.1:c.1825G>T
|
XP_016877584.1:p.Gly609Trp
|
|
XM_017022096.1:c.1696G>T
|
XP_016877585.1:p.Gly566Trp
|
|
XM_017022097.1:c.1687G>T
|
XP_016877586.1:p.Gly563Trp
|
|
XM_017022098.1:c.1492G>T
|
XP_016877587.1:p.Gly498Trp
|
|
NM_002112.4:c.1819G>T
MANE Select
|
NP_002103.2:p.Gly607Trp
|
|
NM_001306146.2:c.1720G>T
|
NP_001293075.1:p.Gly574Trp
|
|