ENST00000224721.12:c.6396C>A
MANE Select
|
ENSP00000224721.9:p.Ile2132=
|
|
ENST00000224721.10:c.6411C>A
|
ENSP00000224721.8:p.Ile2137=
|
|
ENST00000622827.4:c.6396C>A
|
ENSP00000483211.1:p.Ile2132=
|
|
NM_022124.5:c.6396C>A
|
NP_071407.4:p.Ile2132=
|
|
XM_006717940.2:c.6591C>A
|
XP_006718003.1:p.Ile2197=
|
|
XM_006717942.2:c.6525C>A
|
XP_006718005.1:p.Ile2175=
|
|
XM_011540039.1:c.6588C>A
|
XP_011538341.1:p.Ile2196=
|
|
XM_011540040.1:c.6585C>A
|
XP_011538342.1:p.Ile2195=
|
|
XM_011540041.1:c.6531C>A
|
XP_011538343.1:p.Ile2177=
|
|
XM_011540042.1:c.6577+14C>A
|
XP_011538344.1:n.6577+14C>A
|
|
XM_011540043.1:c.6591C>A
|
XP_011538345.1:p.Ile2197=
|
|
XM_011540044.1:c.6456C>A
|
XP_011538346.1:p.Ile2152=
|
|
XM_011540045.1:c.6591C>A
|
XP_011538347.1:p.Ile2197=
|
|
XM_011540046.1:c.6051C>A
|
XP_011538348.1:p.Ile2017=
|
|
XM_011540047.1:c.5409C>A
|
XP_011538349.1:p.Ile1803=
|
|
XM_011540048.1:c.6591C>A
|
XP_011538350.1:p.Ile2197=
|
|
XM_011540049.1:c.6591C>A
|
XP_011538351.1:p.Ile2197=
|
|
XM_011540050.1:c.6591C>A
|
XP_011538352.1:p.Ile2197=
|
|
XM_011540051.1:c.6591C>A
|
XP_011538353.1:p.Ile2197=
|
|
XM_011540052.1:c.2919C>A
|
XP_011538354.1:p.Ile973=
|
|
XR_945796.1:n.6834C>A
|
|
|
NM_022124.6:c.6396C>A
MANE Select
|
NP_071407.4:p.Ile2132=
|
|