ENST00000345317.7:c.199+2112A>T
MANE Select
|
ENSP00000005587.2:n.199+2112A>T
|
|
ENST00000345317.6:c.199+2112A>T
|
ENSP00000005587.2:n.199+2112A>T
|
|
ENST00000432747.1:c.154+2112A>T
|
ENSP00000408163.1:n.154+2112A>T
|
|
ENST00000468712.5:n.360+2112A>T
|
|
|
ENST00000481204.5:n.404+2112A>T
|
|
|
ENST00000487720.1:n.355+2112A>T
|
|
|
ENST00000490456.6:n.372+2112A>T
|
|
|
ENST00000495802.5:n.166+2112A>T
|
|
|
ENST00000497511.5:n.357+2112A>T
|
|
|
NM_001303468.1:c.-318+2112A>T
|
NP_001290397.1:n.-318+2112A>T
|
|
NM_003930.4:c.199+2112A>T
|
NP_003921.2:n.199+2112A>T
|
|
XR_927132.1:n.252-5439T>A
|
|
|
XM_017012771.2:c.199+2112A>T
|
XP_016868260.1:n.199+2112A>T
|
|
NM_003930.5:c.199+2112A>T
MANE Select
|
NP_003921.2:n.199+2112A>T
|
|
NM_001303468.2:c.-318+2112A>T
|
NP_001290397.1:n.-318+2112A>T
|
|