|
ENST00000262304.9:c.12361G>T
MANE Select
|
ENSP00000262304.4:p.Ala4121Ser
|
|
|
ENST00000262304.8:c.12361G>T
|
ENSP00000262304.4:p.Ala4121Ser
|
|
|
ENST00000423118.5:c.12358G>T
|
ENSP00000399501.1:p.Ala4120Ser
|
|
|
ENST00000472577.1:n.389G>T
|
|
|
|
NM_000296.3:c.12358G>T
|
NP_000287.3:p.Ala4120Ser
|
|
|
NM_001009944.2:c.12361G>T
|
NP_001009944.2:p.Ala4121Ser
|
|
|
XM_005255370.2:c.9316G>T
|
XP_005255427.1:p.Ala3106Ser
|
|
|
XM_011522525.1:c.12439G>T
|
XP_011520827.1:p.Ala4147Ser
|
|
|
XM_011522526.1:c.12436G>T
|
XP_011520828.1:p.Ala4146Ser
|
|
|
XM_011522527.1:c.12421G>T
|
XP_011520829.1:p.Ala4141Ser
|
|
|
XM_011522528.1:c.12415G>T
|
XP_011520830.1:p.Ala4139Ser
|
|
|
XM_011522529.1:c.12412G>T
|
XP_011520831.1:p.Ala4138Ser
|
|
|
XM_011522530.1:c.12385G>T
|
XP_011520832.1:p.Ala4129Ser
|
|
|
XM_011522531.1:c.12367G>T
|
XP_011520833.1:p.Ala4123Ser
|
|
|
XM_011522532.1:c.12313G>T
|
XP_011520834.1:p.Ala4105Ser
|
|
|
XM_011522533.1:c.12232G>T
|
XP_011520835.1:p.Ala4078Ser
|
|
|
XM_011522534.1:c.12175G>T
|
XP_011520836.1:p.Ala4059Ser
|
|
|
XM_011522535.1:c.10261G>T
|
XP_011520837.1:p.Ala3421Ser
|
|
|
XM_011522537.1:c.9439G>T
|
XP_011520839.1:p.Ala3147Ser
|
|
|
XR_932867.1:n.12279G>T
|
|
|
|
XM_005255370.3:c.9316G>T
|
XP_005255427.1:p.Ala3106Ser
|
|
|
XM_011522528.3:c.12415G>T
|
XP_011520830.1:p.Ala4139Ser
|
|
|
XM_011522529.2:c.12412G>T
|
XP_011520831.1:p.Ala4138Ser
|
|
|
XM_011522537.2:c.9439G>T
|
XP_011520839.1:p.Ala3147Ser
|
|
|
XM_024450298.1:c.12481G>T
|
XP_024306066.1:p.Ala4161Ser
|
|
|
XM_024450299.1:c.12409G>T
|
XP_024306067.1:p.Ala4137Ser
|
|
|
XM_024450300.1:c.12271G>T
|
XP_024306068.1:p.Ala4091Ser
|
|
|
XM_024450301.1:c.10357G>T
|
XP_024306069.1:p.Ala3453Ser
|
|
|
NM_000296.4:c.12358G>T
|
NP_000287.4:p.Ala4120Ser
|
|
|
NM_001009944.3:c.12361G>T
MANE Select
|
NP_001009944.3:p.Ala4121Ser
|
|
