ENST00000585574.6:c.*166G>C
|
ENSP00000514389.1:n.*166G>C
|
|
ENST00000587504.6:c.687G>C
|
ENSP00000514388.1:p.Leu229=
|
|
ENST00000592386.6:c.726G>C
|
ENSP00000466826.2:p.Leu242=
|
|
ENST00000207549.9:c.744G>C
MANE Select
|
ENSP00000207549.3:p.Leu248=
|
|
ENST00000207549.8:c.744G>C
|
ENSP00000207549.3:p.Leu248=
|
|
ENST00000412096.6:c.744G>C
|
ENSP00000388093.1:p.Leu248=
|
|
ENST00000586147.1:c.117+3705G>C
|
ENSP00000466543.1:n.117+3705G>C
|
|
ENST00000587504.5:n.709G>C
|
|
|
ENST00000590762.5:c.687G>C
|
ENSP00000467653.1:p.Leu229=
|
|
ENST00000591563.5:n.825G>C
|
|
|
ENST00000592386.5:c.723G>C
|
ENSP00000466826.1:p.Leu241=
|
|
NM_199242.2:c.744G>C , LRG_122t1:c.744G>C
|
NP_954712.1:p.Leu248=
|
|
XM_011524504.1:c.744G>C
|
XP_011522806.1:p.Leu248=
|
|
XM_011524505.1:c.744G>C
|
XP_011522807.1:p.Leu248=
|
|
XM_011524506.1:c.744G>C
|
XP_011522808.1:p.Leu248=
|
|
XM_011524507.1:c.135G>C
|
XP_011522809.1:p.Leu45=
|
|
XM_011524508.1:c.135G>C
|
XP_011522810.1:p.Leu45=
|
|
XM_011524504.2:c.744G>C
|
XP_011522806.1:p.Leu248=
|
|
XM_011524507.2:c.135G>C
|
XP_011522809.1:p.Leu45=
|
|
XM_024450640.1:c.135G>C
|
XP_024306408.1:p.Leu45=
|
|
NM_199242.3:c.744G>C
MANE Select
|
NP_954712.1:p.Leu248=
|
|