ENST00000218867.4:c.-51G>T
MANE Select
|
ENSP00000218867.3:n.-51G>T
|
|
ENST00000218867.3:c.-51G>T
|
ENSP00000218867.3:n.-51G>T
|
|
NM_000231.2:c.-51G>T , LRG_207t1:c.-51G>T
|
NP_000222.1:n.-51G>T
|
|
XM_005266505.2:c.-202G>T
|
XP_005266562.1:n.-202G>T
|
|
XM_006719861.2:c.54+20379G>T
|
XP_006719924.1:n.54+20379G>T
|
|
XM_006719861.3:c.54+20379G>T
|
XP_006719924.1:n.54+20379G>T
|
|
XM_024449397.1:c.-152+42G>T
|
XP_024305165.1:n.-152+42G>T
|
|
NM_000231.3:c.-51G>T
MANE Select
|
NP_000222.2:n.-51G>T
|
|
NM_001378244.1:c.54+20379G>T
|
NP_001365173.1:n.54+20379G>T
|
|
NM_001378245.1:c.-152+42G>T
|
NP_001365174.1:n.-152+42G>T
|
|
NM_001378246.1:c.-202G>T
|
NP_001365175.1:n.-202G>T
|
|