ENST00000338883.9:c.3579C>T
MANE Select
|
ENSP00000345629.4:p.His1193=
|
|
ENST00000338883.8:c.3579C>T
|
ENSP00000345629.4:p.His1193=
|
|
ENST00000359173.7:c.2907C>T
|
|
|
ENST00000470101.1:n.997C>T
|
|
|
ENST00000518578.5:n.3641C>T
|
|
|
NM_001001671.3:c.3579C>T
|
NP_001001671.3:p.His1193=
|
|
XM_011545507.1:c.3234C>T
|
XP_011543809.1:p.His1078=
|
|
XM_011545508.1:c.3147C>T
|
XP_011543810.1:p.His1049=
|
|
XM_011545509.1:c.2544C>T
|
XP_011543811.1:p.His848=
|
|
XM_011545510.1:c.2253C>T
|
XP_011543812.1:p.His751=
|
|
XM_011545511.1:c.1884C>T
|
XP_011543813.1:p.His628=
|
|
XM_011545507.3:c.3234C>T
|
XP_011543809.3:p.His1078=
|
|
XM_011545508.3:c.3147C>T
|
XP_011543810.3:p.His1049=
|
|
XM_011545510.2:c.2253C>T
|
XP_011543812.1:p.His751=
|
|
XM_011545511.2:c.1884C>T
|
XP_011543813.1:p.His628=
|
|
NM_001001671.4:c.3579C>T
MANE Select
|
NP_001001671.3:p.His1193=
|
|