ENST00000223051.8:c.726+1G>C
MANE Select
|
ENSP00000223051.3:n.726+1G>C
|
|
ENST00000223051.7:c.726+1G>C
|
ENSP00000223051.3:n.726+1G>C
|
|
ENST00000431692.5:c.726+1G>C
|
ENSP00000413905.1:n.726+1G>C
|
|
ENST00000462107.1:c.726+1G>C
|
ENSP00000420525.1:n.726+1G>C
|
|
ENST00000465294.5:n.731+1G>C
|
|
|
ENST00000473374.5:n.176+1G>C
|
|
|
ENST00000473571.1:n.180+1G>C
|
|
|
ENST00000475011.1:n.255+1G>C
|
|
|
ENST00000476304.5:n.347+1G>C
|
|
|
NM_001206855.1:c.213+1G>C
|
NP_001193784.1:n.213+1G>C
|
|
NM_003227.3:c.726+1G>C
|
NP_003218.2:n.726+1G>C
|
|
XM_005250553.3:c.726+1G>C
|
XP_005250610.1:n.726+1G>C
|
|
XM_005250554.3:c.726+1G>C
|
XP_005250611.1:n.726+1G>C
|
|
NM_001206855.2:c.213+1G>C
|
NP_001193784.1:n.213+1G>C
|
|
XM_005250553.4:c.726+1G>C
|
XP_005250610.1:n.726+1G>C
|
|
XM_017012573.1:c.726+1G>C
|
XP_016868062.1:n.726+1G>C
|
|
NM_003227.4:c.726+1G>C
MANE Select
|
NP_003218.2:n.726+1G>C
|
|
NM_001206855.3:c.213+1G>C
|
NP_001193784.1:n.213+1G>C
|
|