ENST00000389658.4:c.3045C>T
MANE Select
|
ENSP00000374309.3:p.Val1015=
|
|
ENST00000389658.3:c.3045C>T
|
ENSP00000374309.3:p.Val1015=
|
|
ENST00000579014.5:n.4060C>T
|
|
|
NM_005559.3:c.3045C>T
|
NP_005550.2:p.Val1015=
|
|
XM_011525655.1:c.3045C>T
|
XP_011523957.1:p.Val1015=
|
|
XM_011525656.1:c.1473C>T
|
XP_011523958.1:p.Val491=
|
|
XM_011525657.1:c.3045C>T
|
XP_011523959.1:p.Val1015=
|
|
XM_011525655.2:c.3045C>T
|
XP_011523957.1:p.Val1015=
|
|
XM_011525656.2:c.1473C>T
|
XP_011523958.1:p.Val491=
|
|
NM_005559.4:c.3045C>T
MANE Select
|
NP_005550.2:p.Val1015=
|
|