|
ENST00000539696.6:c.-92+7538G>T
|
ENSP00000439134.1:n.-92+7538G>T
|
|
|
ENST00000546277.6:c.388G>T
|
ENSP00000438153.2:p.Asp130Tyr
|
|
|
ENST00000636529.2:n.79-4611G>T
|
|
|
|
ENST00000697195.1:c.*152G>T
|
ENSP00000513181.1:n.*152G>T
|
|
|
ENST00000697196.1:c.388G>T
|
ENSP00000513182.1:p.Asp130Tyr
|
|
|
ENST00000228510.8:c.388G>T
MANE Select
|
ENSP00000228510.3:p.Asp130Tyr
|
|
|
ENST00000636529.1:c.65-4611G>T
|
|
|
|
ENST00000636996.1:c.236G>T
|
|
|
|
ENST00000228510.7:c.388G>T
|
ENSP00000228510.3:p.Asp130Tyr
|
|
|
ENST00000392727.7:c.371+1465G>T
|
ENSP00000376487.3:n.371+1465G>T
|
|
|
ENST00000447878.6:c.227-4611G>T
|
ENSP00000415555.2:n.227-4611G>T
|
|
|
ENST00000535044.1:n.472-4611G>T
|
|
|
|
ENST00000537237.5:c.*152G>T
|
ENSP00000445382.1:n.*152G>T
|
|
|
ENST00000539335.5:c.388G>T
|
ENSP00000440379.1:p.Asp130Tyr
|
|
|
ENST00000539575.4:c.388G>T
|
ENSP00000443551.2:p.Asp130Tyr
|
|
|
ENST00000539696.5:c.-92+7538G>T
|
ENSP00000439134.1:n.-92+7538G>T
|
|
|
ENST00000545774.5:c.227-4611G>T
|
ENSP00000443978.1:n.227-4611G>T
|
|
|
ENST00000546277.5:c.388G>T
|
ENSP00000438153.1:p.Asp130Tyr
|
|
|
ENST00000625889.2:c.371+1465G>T
|
ENSP00000486846.1:n.371+1465G>T
|
|
|
ENST00000629016.2:c.227-4611G>T
|
ENSP00000486804.1:n.227-4611G>T
|
|
|
NM_000431.3:c.388G>T
|
NP_000422.1:p.Asp130Tyr
|
|
|
NM_001114185.2:c.388G>T
|
NP_001107657.1:p.Asp130Tyr
|
|
|
NM_001301182.1:c.371+1465G>T
|
NP_001288111.1:n.371+1465G>T
|
|
|
XM_011538372.1:c.388G>T
|
XP_011536674.1:p.Asp130Tyr
|
|
|
XM_017019313.2:c.371+1465G>T
|
XP_016874802.1:n.371+1465G>T
|
|
|
XM_017019314.1:c.388G>T
|
XP_016874803.1:p.Asp130Tyr
|
|
|
XM_024448982.1:c.388G>T
|
XP_024304750.1:p.Asp130Tyr
|
|
|
NM_000431.4:c.388G>T
MANE Select
|
NP_000422.1:p.Asp130Tyr
|
|
|
NM_001114185.3:c.388G>T
|
NP_001107657.1:p.Asp130Tyr
|
|
|
NM_001301182.2:c.371+1465G>T
|
NP_001288111.1:n.371+1465G>T
|
|
