ENST00000456935.7:c.2923+35G>T
MANE Select
|
ENSP00000395473.2:n.2923+35G>T
|
|
ENST00000221363.8:c.2920+35G>T
|
ENSP00000221363.4:n.2920+35G>T
|
|
ENST00000456935.6:c.2923+35G>T
|
ENSP00000395473.2:n.2923+35G>T
|
|
ENST00000466794.5:n.3513+35G>T
|
|
|
ENST00000469423.1:n.352+35G>T
|
|
|
ENST00000493218.5:n.334+35G>T
|
|
|
ENST00000597692.1:c.482+35G>T
|
|
|
NM_000528.3:c.2923+35G>T
|
NP_000519.2:n.2923+35G>T
|
|
NM_001173498.1:c.2920+35G>T
|
NP_001166969.1:n.2920+35G>T
|
|
XM_005259913.1:c.2926+35G>T
|
XP_005259970.1:n.2926+35G>T
|
|
XM_011528017.1:c.1822+35G>T
|
XP_011526319.1:n.1822+35G>T
|
|
XM_005259913.2:c.2926+35G>T
|
XP_005259970.1:n.2926+35G>T
|
|
XM_024451518.1:c.1822+35G>T
|
XP_024307286.1:n.1822+35G>T
|
|
NM_000528.4:c.2923+35G>T
MANE Select
|
NP_000519.2:n.2923+35G>T
|
|
NM_001173498.2:c.2920+35G>T
|
NP_001166969.1:n.2920+35G>T
|
|