ENST00000375326.9:c.-9G>T
MANE Select
|
ENSP00000364475.5:n.-9G>T
|
|
ENST00000375326.8:c.-9G>T
|
ENSP00000364475.4:n.-9G>T
|
|
ENST00000414122.1:c.-83+725G>T
|
ENSP00000411619.1:n.-83+725G>T
|
|
ENST00000415431.5:c.-9G>T
|
ENSP00000408025.1:n.-9G>T
|
|
NM_000507.3:c.-9G>T
|
NP_000498.2:n.-9G>T
|
|
NM_001127628.1:c.-9G>T
|
NP_001121100.1:n.-9G>T
|
|
XM_006717005.2:c.-77+725G>T
|
XP_006717068.1:n.-77+725G>T
|
|
XM_006717005.4:c.-77+725G>T
|
XP_006717068.1:n.-77+725G>T
|
|
NM_000507.4:c.-9G>T
MANE Select
|
NP_000498.2:n.-9G>T
|
|
NM_001127628.2:c.-9G>T
|
NP_001121100.1:n.-9G>T
|
|