ENST00000356839.10:c.1434+30G>T
MANE Select
|
ENSP00000349297.5:n.1434+30G>T
|
|
ENST00000322910.9:c.*1389+30G>T
|
ENSP00000325395.5:n.*1389+30G>T
|
|
ENST00000350303.9:c.1368+30G>T
|
ENSP00000344152.5:n.1368+30G>T
|
|
ENST00000356839.9:c.1434+30G>T
|
ENSP00000349297.5:n.1434+30G>T
|
|
ENST00000542255.6:c.292+30G>T
|
|
|
ENST00000543245.6:c.1503+30G>T
|
ENSP00000438689.2:n.1503+30G>T
|
|
ENST00000578711.1:n.595G>T
|
|
|
ENST00000579425.5:n.550+30G>T
|
|
|
ENST00000579546.1:c.271+30G>T
|
|
|
ENST00000579894.5:n.175G>T
|
|
|
ENST00000583074.5:n.153+30G>T
|
|
|
ENST00000583850.5:n.209+30G>T
|
|
|
ENST00000583858.5:c.463+30G>T
|
|
|
ENST00000585203.6:n.625+30G>T
|
|
|
NM_000018.3:c.1434+30G>T
|
NP_000009.1:n.1434+30G>T
|
|
NM_001033859.2:c.1368+30G>T
|
NP_001029031.1:n.1368+30G>T
|
|
NM_001270447.1:c.1503+30G>T
|
NP_001257376.1:n.1503+30G>T
|
|
NM_001270448.1:c.1206+30G>T
|
NP_001257377.1:n.1206+30G>T
|
|
XM_006721516.2:c.1434+30G>T
|
XP_006721579.2:n.1434+30G>T
|
|
XM_011523829.1:c.1434+30G>T
|
XP_011522131.1:n.1434+30G>T
|
|
XM_011523830.1:c.1434+30G>T
|
XP_011522132.1:n.1434+30G>T
|
|
XR_934021.1:n.1541+30G>T
|
|
|
XR_934022.1:n.1541+30G>T
|
|
|
XR_934023.1:n.1541+30G>T
|
|
|
XM_006721516.3:c.1434+30G>T
|
XP_006721579.2:n.1434+30G>T
|
|
XM_011523829.2:c.1434+30G>T
|
XP_011522131.1:n.1434+30G>T
|
|
XM_011523830.2:c.1434+30G>T
|
XP_011522132.1:n.1434+30G>T
|
|
XM_024450741.1:c.1434+30G>T
|
XP_024306509.1:n.1434+30G>T
|
|
XR_934021.2:n.1493+30G>T
|
|
|
XR_934022.2:n.1493+30G>T
|
|
|
XR_934023.2:n.1493+30G>T
|
|
|
NM_000018.4:c.1434+30G>T
MANE Select
|
NP_000009.1:n.1434+30G>T
|
|
NM_001033859.3:c.1368+30G>T
|
NP_001029031.1:n.1368+30G>T
|
|
NM_001270447.2:c.1503+30G>T
|
NP_001257376.1:n.1503+30G>T
|
|
NM_001270448.2:c.1206+30G>T
|
NP_001257377.1:n.1206+30G>T
|
|