ENST00000223051.8:c.2136+217C>A
MANE Select
|
ENSP00000223051.3:n.2136+217C>A
|
|
ENST00000223051.7:c.2136+217C>A
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ENSP00000223051.3:n.2136+217C>A
|
|
ENST00000431692.5:c.*811+217C>A
|
ENSP00000413905.1:n.*811+217C>A
|
|
ENST00000462090.5:n.1172+217C>A
|
|
|
ENST00000462107.1:c.2136+217C>A
|
ENSP00000420525.1:n.2136+217C>A
|
|
ENST00000465294.5:n.2056+217C>A
|
|
|
ENST00000476304.5:n.1757+217C>A
|
|
|
ENST00000490084.5:c.1489+217C>A
|
|
|
NM_001206855.1:c.1623+217C>A
|
NP_001193784.1:n.1623+217C>A
|
|
NM_003227.3:c.2136+217C>A
|
NP_003218.2:n.2136+217C>A
|
|
XM_005250553.3:c.2136+217C>A
|
XP_005250610.1:n.2136+217C>A
|
|
XM_005250554.3:c.2214C>A
|
XP_005250611.1:p.Gly738=
|
|
XR_927814.1:n.433+3992G>T
|
|
|
NM_001206855.2:c.1623+217C>A
|
NP_001193784.1:n.1623+217C>A
|
|
XM_005250553.4:c.2136+217C>A
|
XP_005250610.1:n.2136+217C>A
|
|
XM_017012573.1:c.2136+217C>A
|
XP_016868062.1:n.2136+217C>A
|
|
NM_003227.4:c.2136+217C>A
MANE Select
|
NP_003218.2:n.2136+217C>A
|
|
NM_001206855.3:c.1623+217C>A
|
NP_001193784.1:n.1623+217C>A
|
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