ENST00000265104.5:c.9457C>T
MANE Select
|
ENSP00000265104.4:p.Gln3153Ter
|
|
ENST00000681290.1:c.9412C>T
|
ENSP00000505288.1:p.Gln3138Ter
|
|
ENST00000265104.4:c.9457C>T
|
ENSP00000265104.4:p.Gln3153Ter
|
|
ENST00000504001.3:n.169C>T
|
|
|
NM_001369.2:c.9457C>T
|
NP_001360.1:p.Gln3153Ter
|
|
XM_005248262.2:c.9412C>T
|
XP_005248319.1:p.Gln3138Ter
|
|
XM_005248262.3:c.9565C>T
|
XP_005248319.2:p.Gln3189Ter
|
|
XM_017009177.1:c.9565C>T
|
XP_016864666.1:p.Gln3189Ter
|
|
XM_017009178.1:c.8470C>T
|
XP_016864667.1:p.Gln2824Ter
|
|
XM_017009179.2:c.8470C>T
|
XP_016864668.1:p.Gln2824Ter
|
|
XM_017009180.1:c.9565C>T
|
XP_016864669.1:p.Gln3189Ter
|
|
XM_017009181.1:c.9565C>T
|
XP_016864670.1:p.Gln3189Ter
|
|
XM_017009182.1:c.9565C>T
|
XP_016864671.1:p.Gln3189Ter
|
|
XM_017009183.1:c.9565C>T
|
XP_016864672.1:p.Gln3189Ter
|
|
XM_017009185.1:c.4654C>T
|
XP_016864674.1:p.Gln1552Ter
|
|
XM_017009186.1:c.4207C>T
|
XP_016864675.1:p.Gln1403Ter
|
|
XM_017009188.1:c.3544C>T
|
XP_016864677.1:p.Gln1182Ter
|
|
XM_024454388.1:c.8470C>T
|
XP_024310156.1:p.Gln2824Ter
|
|
XM_024454389.1:c.8059C>T
|
XP_024310157.1:p.Gln2687Ter
|
|
NM_001369.3:c.9457C>T
MANE Select
|
NP_001360.1:p.Gln3153Ter
|
|