ENST00000389857.11:c.5088G>T
MANE Select
|
ENSP00000374507.6:p.Leu1696=
|
|
ENST00000331194.8:c.660G>T
|
ENSP00000330332.8:p.Leu220=
|
|
ENST00000334448.5:n.900G>T
|
|
|
ENST00000389857.10:c.5088G>T
|
ENSP00000374507.6:p.Leu1696=
|
|
ENST00000556726.5:c.1316G>T
|
|
|
NM_001080414.3:c.5088G>T
|
NP_001073883.2:p.Leu1696=
|
|
XM_011536796.1:c.4980G>T
|
XP_011535098.1:p.Leu1660=
|
|
XR_429316.2:n.5363G>T
|
|
|
XM_011536796.2:c.4980G>T
|
XP_011535098.1:p.Leu1660=
|
|
XM_017021336.1:c.2169G>T
|
XP_016876825.1:p.Leu723=
|
|
XR_429316.4:n.5361G>T
|
|
|
NM_001080414.4:c.5088G>T
MANE Select
|
NP_001073883.2:p.Leu1696=
|
|