ENST00000705719.1:c.155T>C
|
ENSP00000516165.1:p.Val52Ala
|
|
ENST00000331134.11:c.26T>C
MANE Select
|
ENSP00000331487.5:p.Val9Ala
|
|
ENST00000331134.10:c.26T>C
|
ENSP00000331487.5:p.Val9Ala
|
|
ENST00000374747.9:c.26T>C
|
ENSP00000363879.5:p.Val9Ala
|
|
ENST00000570300.1:n.47T>C
|
|
|
ENST00000574897.5:c.26T>C
|
ENSP00000461543.1:p.Val9Ala
|
|
ENST00000625705.1:c.23T>C
|
ENSP00000486640.1:p.Val8Ala
|
|
NM_017921.3:c.26T>C
|
NP_060391.2:p.Val9Ala
|
|
XM_011524979.1:c.26T>C
|
XP_011523281.1:p.Val9Ala
|
|
XM_011524980.1:c.26T>C
|
XP_011523282.1:p.Val9Ala
|
|
XM_011524981.1:c.26T>C
|
XP_011523283.1:p.Val9Ala
|
|
XM_011524982.1:c.26T>C
|
XP_011523284.1:p.Val9Ala
|
|
XR_934501.1:n.244T>C
|
|
|
XR_934502.1:n.244T>C
|
|
|
XM_011524982.2:c.26T>C
|
XP_011523284.1:p.Val9Ala
|
|
XR_001752557.1:n.244T>C
|
|
|
NM_017921.4:c.26T>C
MANE Select
|
NP_060391.2:p.Val9Ala
|
|
NM_001369698.1:c.26T>C
|
NP_001356627.1:p.Val9Ala
|
|