ENST00000356839.10:c.878+181A>T
MANE Select
|
ENSP00000349297.5:n.878+181A>T
|
|
ENST00000322910.9:c.*833+181A>T
|
ENSP00000325395.5:n.*833+181A>T
|
|
ENST00000350303.9:c.812+181A>T
|
ENSP00000344152.5:n.812+181A>T
|
|
ENST00000356839.9:c.878+181A>T
|
ENSP00000349297.5:n.878+181A>T
|
|
ENST00000543245.6:c.947+181A>T
|
ENSP00000438689.2:n.947+181A>T
|
|
ENST00000581378.5:c.596+181A>T
|
|
|
ENST00000582379.1:n.262+181A>T
|
|
|
NM_000018.3:c.878+181A>T
|
NP_000009.1:n.878+181A>T
|
|
NM_001033859.2:c.812+181A>T
|
NP_001029031.1:n.812+181A>T
|
|
NM_001270447.1:c.947+181A>T
|
NP_001257376.1:n.947+181A>T
|
|
NM_001270448.1:c.650+181A>T
|
NP_001257377.1:n.650+181A>T
|
|
XM_006721516.2:c.878+181A>T
|
XP_006721579.2:n.878+181A>T
|
|
XM_011523829.1:c.878+181A>T
|
XP_011522131.1:n.878+181A>T
|
|
XM_011523830.1:c.878+181A>T
|
XP_011522132.1:n.878+181A>T
|
|
XR_934021.1:n.985+181A>T
|
|
|
XR_934022.1:n.985+181A>T
|
|
|
XR_934023.1:n.985+181A>T
|
|
|
XM_006721516.3:c.878+181A>T
|
XP_006721579.2:n.878+181A>T
|
|
XM_011523829.2:c.878+181A>T
|
XP_011522131.1:n.878+181A>T
|
|
XM_011523830.2:c.878+181A>T
|
XP_011522132.1:n.878+181A>T
|
|
XM_024450741.1:c.878+181A>T
|
XP_024306509.1:n.878+181A>T
|
|
XR_934021.2:n.937+181A>T
|
|
|
XR_934022.2:n.937+181A>T
|
|
|
XR_934023.2:n.937+181A>T
|
|
|
NM_000018.4:c.878+181A>T
MANE Select
|
NP_000009.1:n.878+181A>T
|
|
NM_001033859.3:c.812+181A>T
|
NP_001029031.1:n.812+181A>T
|
|
NM_001270447.2:c.947+181A>T
|
NP_001257376.1:n.947+181A>T
|
|
NM_001270448.2:c.650+181A>T
|
NP_001257377.1:n.650+181A>T
|
|