ENST00000570803.6:c.-36G=
|
ENSP00000460543.2:n.-36G=
|
|
ENST00000572080.2:c.-116G=
|
ENSP00000459972.2:n.-116G=
|
|
ENST00000577106.6:c.-151G=
|
ENSP00000458306.2:n.-151G=
|
|
ENST00000302262.8:c.-301G=
MANE Select
|
ENSP00000305692.3:n.-301G=
|
|
ENST00000390015.7:c.-116G=
|
ENSP00000374665.3:n.-116G=
|
|
ENST00000570803.5:c.-36G=
|
ENSP00000460543.1:n.-36G=
|
|
ENST00000574376.1:n.26G=
|
|
|
ENST00000577106.5:c.-151G=
|
ENSP00000458306.1:n.-151G=
|
|
NM_000152.3:c.-301G= , LRG_673t1:c.-301G=
|
NP_000143.2:n.-301G=
|
|
NM_001079803.1:c.-116G=
|
NP_001073271.1:n.-116G=
|
|
NM_001079804.1:c.-36G=
|
NP_001073272.1:n.-36G=
|
|
XM_005257193.1:c.-211G=
|
XP_005257250.1:n.-211G=
|
|
XM_005257194.3:c.-151G=
|
XP_005257251.1:n.-151G=
|
|
NM_000152.4:c.-301G=
|
NP_000143.2:n.-301G=
|
|
NM_001079803.2:c.-116G=
|
NP_001073271.1:n.-116G=
|
|
NM_001079804.2:c.-36G=
|
NP_001073272.1:n.-36G=
|
|
NR_134848.1:n.97G=
|
|
|
XM_005257194.4:c.-151G=
|
XP_005257251.1:n.-151G=
|
|
NM_000152.5:c.-301G=
MANE Select
|
NP_000143.2:n.-301G=
|
|
NM_001079803.3:c.-116G=
|
NP_001073271.1:n.-116G=
|
|
NM_001079804.3:c.-36G=
|
NP_001073272.1:n.-36G=
|
|
NR_134848.2:n.42G=
|
|
|