|
ENST00000356839.10:c.622+41T>G
MANE Select
|
ENSP00000349297.5:n.622+41T>G
|
|
|
ENST00000322910.9:c.*577+41T>G
|
ENSP00000325395.5:n.*577+41T>G
|
|
|
ENST00000350303.9:c.556+41T>G
|
ENSP00000344152.5:n.556+41T>G
|
|
|
ENST00000356839.9:c.622+41T>G
|
ENSP00000349297.5:n.622+41T>G
|
|
|
ENST00000543245.6:c.691+41T>G
|
ENSP00000438689.2:n.691+41T>G
|
|
|
ENST00000577191.5:n.699+41T>G
|
|
|
|
ENST00000577857.5:n.438+41T>G
|
|
|
|
ENST00000579286.5:n.803+41T>G
|
|
|
|
ENST00000579886.2:c.460+41T>G
|
ENSP00000463246.1:n.460+41T>G
|
|
|
ENST00000580365.1:n.353+41T>G
|
|
|
|
ENST00000581378.5:c.340+41T>G
|
|
|
|
ENST00000581562.5:n.525-229T>G
|
|
|
|
ENST00000583312.5:c.622+41T>G
|
ENSP00000467920.1:n.622+41T>G
|
|
|
ENST00000583760.1:n.404+41T>G
|
|
|
|
NM_000018.3:c.622+41T>G
|
NP_000009.1:n.622+41T>G
|
|
|
NM_001033859.2:c.556+41T>G
|
NP_001029031.1:n.556+41T>G
|
|
|
NM_001270447.1:c.691+41T>G
|
NP_001257376.1:n.691+41T>G
|
|
|
NM_001270448.1:c.394+41T>G
|
NP_001257377.1:n.394+41T>G
|
|
|
XM_006721516.2:c.622+41T>G
|
XP_006721579.2:n.622+41T>G
|
|
|
XM_011523829.1:c.622+41T>G
|
XP_011522131.1:n.622+41T>G
|
|
|
XM_011523830.1:c.622+41T>G
|
XP_011522132.1:n.622+41T>G
|
|
|
XR_934021.1:n.729+41T>G
|
|
|
|
XR_934022.1:n.729+41T>G
|
|
|
|
XR_934023.1:n.729+41T>G
|
|
|
|
XM_006721516.3:c.622+41T>G
|
XP_006721579.2:n.622+41T>G
|
|
|
XM_011523829.2:c.622+41T>G
|
XP_011522131.1:n.622+41T>G
|
|
|
XM_011523830.2:c.622+41T>G
|
XP_011522132.1:n.622+41T>G
|
|
|
XM_024450741.1:c.622+41T>G
|
XP_024306509.1:n.622+41T>G
|
|
|
XR_934021.2:n.681+41T>G
|
|
|
|
XR_934022.2:n.681+41T>G
|
|
|
|
XR_934023.2:n.681+41T>G
|
|
|
|
NM_000018.4:c.622+41T>G
MANE Select
|
NP_000009.1:n.622+41T>G
|
|
|
NM_001033859.3:c.556+41T>G
|
NP_001029031.1:n.556+41T>G
|
|
|
NM_001270447.2:c.691+41T>G
|
NP_001257376.1:n.691+41T>G
|
|
|
NM_001270448.2:c.394+41T>G
|
NP_001257377.1:n.394+41T>G
|
|
