ENST00000218867.4:c.-56G=
MANE Select
|
ENSP00000218867.3:n.-56G=
|
|
ENST00000218867.3:c.-56G=
|
ENSP00000218867.3:n.-56G=
|
|
NM_000231.2:c.-56G= , LRG_207t1:c.-56G=
|
NP_000222.1:n.-56G=
|
|
XM_005266505.2:c.-207G=
|
XP_005266562.1:n.-207G=
|
|
XM_006719861.2:c.54+20374G=
|
XP_006719924.1:n.54+20374G=
|
|
XM_006719861.3:c.54+20374G=
|
XP_006719924.1:n.54+20374G=
|
|
XM_024449397.1:c.-152+37G=
|
XP_024305165.1:n.-152+37G=
|
|
NM_000231.3:c.-56G=
MANE Select
|
NP_000222.2:n.-56G=
|
|
NM_001378244.1:c.54+20374G=
|
NP_001365173.1:n.54+20374G=
|
|
NM_001378245.1:c.-152+37G=
|
NP_001365174.1:n.-152+37G=
|
|
NM_001378246.1:c.-207G=
|
NP_001365175.1:n.-207G=
|
|