|
ENST00000358552.8:c.556+1G>A
|
ENSP00000351354.5:n.556+1G>A
|
|
|
ENST00000622520.2:c.556+1G>A
|
ENSP00000481181.2:n.556+1G>A
|
|
|
ENST00000693124.1:c.377+1G>A
|
|
|
|
ENST00000592199.6:c.559+1G>A
MANE Select
|
ENSP00000467512.1:n.559+1G>A
|
|
|
ENST00000676441.1:c.583+1G>A
|
ENSP00000502554.1:n.583+1G>A
|
|
|
ENST00000358552.7:c.568+1G>A
|
ENSP00000351354.4:n.568+1G>A
|
|
|
ENST00000360105.8:c.568+1G>A
|
ENSP00000353219.4:n.568+1G>A
|
|
|
ENST00000397661.6:c.559+1G>A
|
ENSP00000380781.2:n.559+1G>A
|
|
|
ENST00000585382.5:c.234+185G>A
|
ENSP00000466605.1:n.234+185G>A
|
|
|
ENST00000585575.5:c.535+1G>A
|
ENSP00000468794.1:n.535+1G>A
|
|
|
ENST00000586797.5:c.*390+1G>A
|
ENSP00000467536.1:n.*390+1G>A
|
|
|
ENST00000587260.1:c.556+1G>A
|
ENSP00000467785.1:n.556+1G>A
|
|
|
ENST00000587760.5:c.535+1G>A
|
ENSP00000466389.1:n.535+1G>A
|
|
|
ENST00000588228.5:c.418+1G>A
|
ENSP00000466735.1:n.418+1G>A
|
|
|
ENST00000592199.5:c.559+1G>A
|
ENSP00000467512.1:n.559+1G>A
|
|
|
NM_001271043.2:c.583+1G>A
|
NP_001257972.1:n.583+1G>A
|
|
|
NM_001271044.2:c.535+1G>A
|
NP_001257973.1:n.535+1G>A
|
|
|
NM_002501.3:c.559+1G>A
|
NP_002492.2:n.559+1G>A
|
|
|
XM_005259917.3:c.736+1G>A
|
XP_005259974.1:n.736+1G>A
|
|
|
XM_005259918.3:c.559+1G>A
|
XP_005259975.1:n.559+1G>A
|
|
|
XM_005259919.3:c.736+1G>A
|
XP_005259976.1:n.736+1G>A
|
|
|
XM_005259920.3:c.535+1G>A
|
XP_005259977.1:n.535+1G>A
|
|
|
XM_005259921.3:c.736+1G>A
|
XP_005259978.1:n.736+1G>A
|
|
|
XM_005259922.3:c.736+1G>A
|
XP_005259979.1:n.736+1G>A
|
|
|
XM_006722760.2:c.736+1G>A
|
XP_006722823.1:n.736+1G>A
|
|
|
XM_011528040.1:c.607+1G>A
|
XP_011526342.1:n.607+1G>A
|
|
|
NM_001365902.1:c.559+1G>A
|
NP_001352831.1:n.559+1G>A
|
|
|
NM_001365982.1:c.559+1G>A
|
NP_001352911.1:n.559+1G>A
|
|
|
NM_001365983.1:c.418+1G>A
|
NP_001352912.1:n.418+1G>A
|
|
|
NM_001365984.1:c.556+1G>A
|
NP_001352913.1:n.556+1G>A
|
|
|
NM_001365985.1:c.556+1G>A
|
NP_001352914.1:n.556+1G>A
|
|
|
XM_005259917.4:c.736+1G>A
|
XP_005259974.1:n.736+1G>A
|
|
|
NM_001271044.3:c.535+1G>A
|
NP_001257973.1:n.535+1G>A
|
|
|
NM_001365902.2:c.559+1G>A
|
NP_001352831.1:n.559+1G>A
|
|
|
NM_001365982.2:c.559+1G>A
|
NP_001352911.1:n.559+1G>A
|
|
|
NM_001365983.2:c.418+1G>A
|
NP_001352912.1:n.418+1G>A
|
|
|
NM_001365984.2:c.556+1G>A
|
NP_001352913.1:n.556+1G>A
|
|
|
NM_001365985.2:c.556+1G>A
|
NP_001352914.1:n.556+1G>A
|
|
|
NM_002501.4:c.559+1G>A
|
NP_002492.2:n.559+1G>A
|
|
|
NM_001365902.3:c.559+1G>A
MANE Select
|
NP_001352831.1:n.559+1G>A
|
|
|
NM_001378404.1:c.535+1G>A
|
NP_001365333.1:n.535+1G>A
|
|
|
NM_001378405.1:c.607+1G>A
|
NP_001365334.1:n.607+1G>A
|
|
