ENST00000698355.1:c.177G>T
|
ENSP00000513678.1:p.Val59=
|
|
ENST00000698356.1:c.177G>T
|
ENSP00000513679.1:p.Val59=
|
|
ENST00000698357.1:c.177G>T
|
ENSP00000513680.1:p.Val59=
|
|
ENST00000367568.5:c.177G>T
MANE Select
|
ENSP00000356540.4:p.Val59=
|
|
ENST00000367568.4:c.177G>T
|
ENSP00000356540.4:p.Val59=
|
|
NM_003764.3:c.177G>T , LRG_113t1:c.177G>T
|
NP_003755.2:p.Val59=
|
|
XM_011536213.1:c.255G>T
|
XP_011534515.1:p.Val85=
|
|
XM_011536214.1:c.177G>T
|
XP_011534516.1:p.Val59=
|
|
XM_011536215.1:c.177G>T
|
XP_011534517.1:p.Val59=
|
|
XM_011536216.1:c.177G>T
|
XP_011534518.1:p.Val59=
|
|
XM_011536217.1:c.177G>T
|
XP_011534519.1:p.Val59=
|
|
XM_011536218.1:c.177G>T
|
XP_011534520.1:p.Val59=
|
|
XM_011536213.2:c.255G>T
|
XP_011534515.1:p.Val85=
|
|
XM_011536214.2:c.177G>T
|
XP_011534516.1:p.Val59=
|
|
XM_011536217.2:c.177G>T
|
XP_011534519.1:p.Val59=
|
|
XM_011536218.2:c.177G>T
|
XP_011534520.1:p.Val59=
|
|
XM_017011400.1:c.177G>T
|
XP_016866889.1:p.Val59=
|
|
NM_003764.4:c.177G>T
MANE Select
|
NP_003755.2:p.Val59=
|
|