|
ENST00000265077.8:c.9104C>T
(VCAN)
MANE Select
|
ENSP00000265077.3:p.Ala3035Val
|
|
|
ENST00000265077.7:c.9104C>T
(VCAN)
|
ENSP00000265077.3:p.Ala3035Val
|
|
|
ENST00000342785.8:c.4004-3430C>T
(VCAN)
|
ENSP00000342768.4:n.4004-3430C>T
|
|
|
ENST00000343200.9:c.6143C>T
(VCAN)
|
ENSP00000340062.5:p.Ala2048Val
|
|
|
ENST00000502527.2:c.1043-3430C>T
(VCAN)
|
ENSP00000421362.2:n.1043-3430C>T
|
|
|
ENST00000507162.1:n.160C>T
(VCAN)
|
|
|
|
ENST00000512590.6:c.3860-3430C>T
(VCAN)
|
ENSP00000425959.2:n.3860-3430C>T
|
|
|
ENST00000513016.5:n.6494C>T
(VCAN)
|
|
|
|
NM_001126336.2:c.1043-3430C>T
(VCAN)
|
NP_001119808.1:n.1043-3430C>T
|
|
|
NM_001164097.1:c.6143C>T
(VCAN)
|
NP_001157569.1:p.Ala2048Val
|
|
|
NM_001164098.1:c.4004-3430C>T
(VCAN)
|
NP_001157570.1:n.4004-3430C>T
|
|
|
NM_004385.4:c.9104C>T
(VCAN)
|
NP_004376.2:p.Ala3035Val
|
|
|
XM_011543776.1:c.161-7925G>A
(VCAN-AS1)
|
XP_011542078.1:n.161-7925G>A
|
|
|
XM_011543777.1:c.161-7934G>A
(VCAN-AS1)
|
XP_011542079.1:n.161-7934G>A
|
|
|
XM_011543778.1:c.161-7925G>A
(VCAN-AS1)
|
XP_011542080.1:n.161-7925G>A
|
|
|
XM_011543779.1:c.161-7925G>A
(VCAN-AS1)
|
XP_011542081.1:n.161-7925G>A
|
|
|
XM_011543780.1:c.13-7934G>A
(VCAN-AS1)
|
XP_011542082.1:n.13-7934G>A
|
|
|
XM_011543781.1:c.161-7925G>A
(VCAN-AS1)
|
XP_011542083.1:n.161-7925G>A
|
|
|
XM_011543782.1:c.161-7925G>A
(VCAN-AS1)
|
XP_011542084.1:n.161-7925G>A
|
|
|
XR_948512.1:n.471-7925G>A
(VCAN-AS1)
|
|
|
|
XR_948513.1:n.471-7934G>A
(VCAN-AS1)
|
|
|
|
XR_948514.1:n.471-7925G>A
(VCAN-AS1)
|
|
|
|
XR_948515.1:n.471-7934G>A
(VCAN-AS1)
|
|
|
|
XR_948516.1:n.471-7934G>A
(VCAN-AS1)
|
|
|
|
NR_136215.1:n.285-7934G>A
(VCAN-AS1)
|
|
|
|
NM_004385.5:c.9104C>T
(VCAN)
MANE Select
|
NP_004376.2:p.Ala3035Val
|
|
|
NM_001126336.3:c.1043-3430C>T
(VCAN)
|
NP_001119808.1:n.1043-3430C>T
|
|
|
NM_001164097.2:c.6143C>T
(VCAN)
|
NP_001157569.1:p.Ala2048Val
|
|
|
NM_001164098.2:c.4004-3430C>T
(VCAN)
|
NP_001157570.1:n.4004-3430C>T
|
|
