ENST00000460680.6:c.2076G=
MANE Select
|
ENSP00000417132.1:p.Val692=
|
|
ENST00000296288.9:c.2022G=
|
ENSP00000296288.5:p.Val674=
|
|
ENST00000460680.5:c.2076G=
|
ENSP00000417132.1:p.Val692=
|
|
ENST00000466093.1:n.749G=
|
|
|
ENST00000469613.5:c.275G=
|
|
|
ENST00000478368.1:c.648G=
|
ENSP00000420647.1:p.Val216=
|
|
NM_004656.3:c.2076G=
|
NP_004647.1:p.Val692=
|
|
XM_011534149.1:c.2145G=
|
XP_011532451.1:p.Val715=
|
|
XM_011534150.1:c.2100G=
|
XP_011532452.1:p.Val700=
|
|
XM_011534151.1:c.2091G=
|
XP_011532453.1:p.Val697=
|
|
XM_011534152.1:c.2031G=
|
XP_011532454.1:p.Val677=
|
|
XM_011534149.3:c.2145G=
|
XP_011532451.1:p.Val715=
|
|
XM_011534150.3:c.2100G=
|
XP_011532452.1:p.Val700=
|
|
XM_011534151.3:c.2091G=
|
XP_011532453.1:p.Val697=
|
|
XM_011534152.2:c.2031G=
|
XP_011532454.1:p.Val677=
|
|
XM_017007303.2:c.2022G=
|
XP_016862792.1:p.Val674=
|
|
NM_004656.4:c.2076G=
MANE Select
|
NP_004647.1:p.Val692=
|
|