ENST00000332142.10:c.1709G=
MANE Select
|
ENSP00000331727.5:p.Trp570=
|
|
ENST00000328032.8:c.1688G=
|
ENSP00000333781.4:p.Trp563=
|
|
ENST00000332142.9:c.1709G=
|
ENSP00000331727.5:p.Trp570=
|
|
ENST00000618399.4:c.1409G=
|
ENSP00000482818.1:p.Trp470=
|
|
ENST00000621889.1:c.1382G=
|
ENSP00000483158.1:p.Trp461=
|
|
NM_033272.3:c.1709G=
|
NP_150375.2:p.Trp570=
|
|
NM_173162.2:c.1688G=
|
NP_775185.1:p.Trp563=
|
|
XM_011512109.1:c.1733G=
|
XP_011510411.1:p.Trp578=
|
|
XM_011512109.3:c.1733G=
|
XP_011510411.1:p.Trp578=
|
|
XM_017005218.2:c.1733G=
|
XP_016860707.1:p.Trp578=
|
|
XM_017005219.2:c.1709G=
|
XP_016860708.1:p.Trp570=
|
|
XM_017005220.2:c.1688G=
|
XP_016860709.1:p.Trp563=
|
|
XM_017005221.2:c.1733G=
|
XP_016860710.1:p.Trp578=
|
|
NM_033272.4:c.1709G=
MANE Select
|
NP_150375.2:p.Trp570=
|
|
NM_173162.3:c.1688G=
|
NP_775185.1:p.Trp563=
|
|