ENST00000700061.1:c.1055T>A
|
|
|
ENST00000700062.1:c.1055T>A
|
|
|
ENST00000700065.1:n.2971T>A
|
|
|
ENST00000281513.10:c.2958T>A
MANE Select
|
ENSP00000281513.5:p.Pro986=
|
|
ENST00000281513.9:c.2958T>A
|
ENSP00000281513.5:p.Pro986=
|
|
ENST00000429842.1:c.250T>A
|
|
|
ENST00000441755.5:c.99T>A
|
ENSP00000396501.1:p.Pro33=
|
|
ENST00000442506.5:c.101T>A
|
|
|
NM_015909.3:c.2958T>A
|
NP_056993.2:p.Pro986=
|
|
NR_052013.2:n.3002T>A
|
|
|
XM_011510357.1:c.2829T>A
|
XP_011508659.1:p.Pro943=
|
|
XM_011510358.1:c.2958T>A
|
XP_011508660.1:p.Pro986=
|
|
XM_011510359.1:c.2319T>A
|
XP_011508661.1:p.Pro773=
|
|
XM_011510360.1:c.759T>A
|
XP_011508662.1:p.Pro253=
|
|
XM_011510361.1:c.750T>A
|
XP_011508663.1:p.Pro250=
|
|
XM_011510357.2:c.2829T>A
|
XP_011508659.1:p.Pro943=
|
|
XM_011510358.2:c.2958T>A
|
XP_011508660.1:p.Pro986=
|
|
XM_011510360.2:c.759T>A
|
XP_011508662.1:p.Pro253=
|
|
XM_011510361.2:c.750T>A
|
XP_011508663.1:p.Pro250=
|
|
XM_017004317.1:c.2958T>A
|
XP_016859806.1:p.Pro986=
|
|
XM_024452961.1:c.2319T>A
|
XP_024308729.1:p.Pro773=
|
|
NM_015909.4:c.2958T>A
MANE Select
|
NP_056993.2:p.Pro986=
|
|
NR_052013.3:n.2988T>A
|
|
|