ENST00000700061.1:c.526T>C
|
|
|
ENST00000700062.1:c.526T>C
|
|
|
ENST00000700065.1:n.2442T>C
|
|
|
ENST00000700066.1:c.1946T>C
|
ENSP00000514780.1:p.Val649Ala
|
|
ENST00000281513.10:c.2429T>C
MANE Select
|
ENSP00000281513.5:p.Val810Ala
|
|
ENST00000281513.9:c.2429T>C
|
ENSP00000281513.5:p.Val810Ala
|
|
NM_015909.3:c.2429T>C
|
NP_056993.2:p.Val810Ala
|
|
NR_052013.2:n.2473T>C
|
|
|
XM_011510357.1:c.2300T>C
|
XP_011508659.1:p.Val767Ala
|
|
XM_011510358.1:c.2429T>C
|
XP_011508660.1:p.Val810Ala
|
|
XM_011510359.1:c.1790T>C
|
XP_011508661.1:p.Val597Ala
|
|
XM_011510360.1:c.230T>C
|
XP_011508662.1:p.Val77Ala
|
|
XM_011510361.1:c.221T>C
|
XP_011508663.1:p.Val74Ala
|
|
XM_011510357.2:c.2300T>C
|
XP_011508659.1:p.Val767Ala
|
|
XM_011510358.2:c.2429T>C
|
XP_011508660.1:p.Val810Ala
|
|
XM_011510360.2:c.230T>C
|
XP_011508662.1:p.Val77Ala
|
|
XM_011510361.2:c.221T>C
|
XP_011508663.1:p.Val74Ala
|
|
XM_017004317.1:c.2429T>C
|
XP_016859806.1:p.Val810Ala
|
|
XM_024452961.1:c.1790T>C
|
XP_024308729.1:p.Val597Ala
|
|
NM_015909.4:c.2429T>C
MANE Select
|
NP_056993.2:p.Val810Ala
|
|
NR_052013.3:n.2459T>C
|
|
|