|
NM_000287.4:c.1206C>T
MANE Select
|
NP_000278.3:p.Ala402=
|
|
ENST00000304611.13:c.1206C>T
MANE Select
|
ENSP00000303511.8:p.Ala402=
|
|
NM_000287.3:c.1206C>T
|
NP_000278.3:p.Ala402=
|
|
NM_001316313.1:c.942C>T
|
NP_001303242.1:p.Ala314=
|
|
NM_001316313.2:c.942C>T
|
NP_001303242.1:p.Ala314=
|
|
NR_133009.1:n.1299C>T
|
|
|
NR_133009.2:n.1237C>T
|
|
|
ENST00000244546.4:c.1206C>T
|
ENSP00000244546.4:p.Ala402=
|
|
ENST00000304611.12:c.1206C>T
|
ENSP00000303511.8:p.Ala402=
|
|
XM_011514661.1:c.1122C>T
|
XP_011512963.1:p.Ala374=
|
|
XM_011514661.2:c.1122C>T
|
XP_011512963.1:p.Ala374=
|
|
XR_001743466.2:n.2280C>T
|
|
|
XR_926246.1:n.1299C>T
|
|