ENST00000342741.6:c.792G>T
MANE Select
|
ENSP00000339933.4:p.Leu264=
|
|
ENST00000342741.4:c.792G>T
|
ENSP00000339933.4:p.Leu264=
|
|
ENST00000392414.7:c.699G>T
|
ENSP00000376214.3:p.Leu233=
|
|
NM_000298.5:c.792G>T
|
NP_000289.1:p.Leu264=
|
|
NM_181871.3:c.699G>T
|
NP_870986.1:p.Leu233=
|
|
XM_005245266.3:c.951G>T
|
XP_005245323.1:p.Leu317=
|
|
XM_006711386.2:c.600G>T
|
XP_006711449.1:p.Leu200=
|
|
XM_011509639.1:c.951G>T
|
XP_011507941.1:p.Leu317=
|
|
XM_011509640.1:c.600G>T
|
XP_011507942.1:p.Leu200=
|
|
NM_000298.6:c.792G>T
MANE Select
|
NP_000289.1:p.Leu264=
|
|
XM_006711386.4:c.600G>T
|
XP_006711449.1:p.Leu200=
|
|
XM_011509640.3:c.600G>T
|
XP_011507942.1:p.Leu200=
|
|
XM_017001493.1:c.792G>T
|
XP_016856982.1:p.Leu264=
|
|
NM_181871.4:c.699G>T
|
NP_870986.1:p.Leu233=
|
|