ENST00000399503.4:c.708C=
MANE Select
|
ENSP00000382423.3:p.Val236=
|
|
ENST00000399503.3:c.708C=
|
ENSP00000382423.3:p.Val236=
|
|
NM_005921.1:c.708C=
|
NP_005912.1:p.Val236=
|
|
XM_005248519.3:c.330C=
|
XP_005248576.2:p.Val110=
|
|
XM_011543406.1:c.453C=
|
XP_011541708.1:p.Val151=
|
|
XM_011543407.1:c.708C=
|
XP_011541709.1:p.Val236=
|
|
XM_011543408.1:c.708C=
|
XP_011541710.1:p.Val236=
|
|
XM_017009484.1:c.297C=
|
XP_016864973.1:p.Val99=
|
|
XM_017009485.1:c.219C=
|
XP_016864974.1:p.Val73=
|
|
XR_001742068.2:n.739C=
|
|
|
NM_005921.2:c.708C=
MANE Select
|
NP_005912.1:p.Val236=
|
|