ENST00000370314.9:c.551+9951G>A
MANE Select
|
ENSP00000359337.4:n.551+9951G>A
|
|
ENST00000370314.8:c.551+9951G>A
|
ENSP00000359337.4:n.551+9951G>A
|
|
ENST00000535043.1:c.551+9951G>A
|
ENSP00000443527.1:n.551+9951G>A
|
|
NM_000808.3:c.551+9951G>A
|
NP_000799.1:n.551+9951G>A
|
|
XM_005274659.1:c.551+9951G>A
|
XP_005274716.1:n.551+9951G>A
|
|
XM_006724811.1:c.551+9951G>A
|
XP_006724874.1:n.551+9951G>A
|
|
XM_011531133.1:c.551+9951G>A
|
XP_011529435.1:n.551+9951G>A
|
|
XM_011531134.1:c.551+9951G>A
|
XP_011529436.1:n.551+9951G>A
|
|
XM_006724811.3:c.551+9951G>A
|
XP_006724874.1:n.551+9951G>A
|
|
NM_000808.4:c.551+9951G>A
MANE Select
|
NP_000799.1:n.551+9951G>A
|
|