ENST00000352689.11:c.98+8377G>A
MANE Select
|
ENSP00000323527.6:n.98+8377G>A
|
|
ENST00000352689.10:c.98+8377G>A
|
ENSP00000323527.6:n.98+8377G>A
|
|
ENST00000416992.6:c.-178-39050G>A
|
ENSP00000387920.1:n.-178-39050G>A
|
|
ENST00000421797.6:c.-178-39050G>A
|
ENSP00000398094.2:n.-178-39050G>A
|
|
ENST00000429546.5:c.-178-39050G>A
|
ENSP00000399954.1:n.-178-39050G>A
|
|
ENST00000446815.5:c.-109+8377G>A
|
ENSP00000412815.1:n.-109+8377G>A
|
|
ENST00000458153.5:c.98+8377G>A
|
ENSP00000407705.1:n.98+8377G>A
|
|
ENST00000494286.5:n.142+8377G>A
|
|
|
ENST00000494785.5:n.115+8377G>A
|
|
|
NM_001145354.1:c.30-39050G>A
|
NP_001138826.1:n.30-39050G>A
|
|
NM_013255.4:c.98+8377G>A
|
NP_037387.2:n.98+8377G>A
|
|
XM_006715993.1:c.98+8377G>A
|
XP_006716056.1:n.98+8377G>A
|
|
XM_011516224.1:c.98+8377G>A
|
XP_011514526.1:n.98+8377G>A
|
|
NM_001321316.1:c.-527+8377G>A
|
NP_001308245.1:n.-527+8377G>A
|
|
XM_006715993.3:c.98+8377G>A
|
XP_006716056.1:n.98+8377G>A
|
|
XM_011516224.3:c.98+8377G>A
|
XP_011514526.1:n.98+8377G>A
|
|
XM_024446766.1:c.-216+8377G>A
|
XP_024302534.1:n.-216+8377G>A
|
|
XM_024446767.1:c.-178-39050G>A
|
XP_024302535.1:n.-178-39050G>A
|
|
NM_013255.5:c.98+8377G>A
MANE Select
|
NP_037387.2:n.98+8377G>A
|
|
NM_001145354.2:c.30-39050G>A
|
NP_001138826.1:n.30-39050G>A
|
|
NM_001321316.2:c.-527+8377G>A
|
NP_001308245.1:n.-527+8377G>A
|
|