ENST00000382103.7:c.952C>G
MANE Select
|
ENSP00000371535.2:p.Pro318Ala
|
|
ENST00000680581.1:c.952C>G
|
ENSP00000506483.1:p.Pro318Ala
|
|
ENST00000680824.1:n.2168C>G
|
|
|
ENST00000681071.1:n.1244C>G
|
|
|
ENST00000681341.1:n.2093C>G
|
|
|
ENST00000681948.1:c.1207C>G
|
ENSP00000505991.1:p.Pro403Ala
|
|
ENST00000358971.7:c.*750C>G
|
ENSP00000351857.3:n.*750C>G
|
|
ENST00000382103.6:c.952C>G
|
ENSP00000371535.2:p.Pro318Ala
|
|
ENST00000503150.1:c.234C>G
|
|
|
ENST00000505513.1:n.252C>G
|
|
|
ENST00000514585.5:c.*653C>G
|
ENSP00000421880.1:n.*653C>G
|
|
NM_016955.3:c.952C>G
|
NP_058651.3:p.Pro318Ala
|
|
XM_005248168.2:c.715C>G
|
XP_005248225.1:p.Pro239Ala
|
|
XM_006713965.2:c.772C>G
|
XP_006714028.1:p.Pro258Ala
|
|
XM_011513846.1:c.949C>G
|
XP_011512148.1:p.Pro317Ala
|
|
XM_011513847.1:c.919C>G
|
XP_011512149.1:p.Pro307Ala
|
|
XM_011513848.1:c.772C>G
|
XP_011512150.1:p.Pro258Ala
|
|
XM_011513846.2:c.949C>G
|
XP_011512148.1:p.Pro317Ala
|
|
XM_011513847.2:c.919C>G
|
XP_011512149.1:p.Pro307Ala
|
|
XM_017008277.1:c.1207C>G
|
XP_016863766.1:p.Pro403Ala
|
|
XM_017008278.1:c.529C>G
|
XP_016863767.1:p.Pro177Ala
|
|
NM_016955.4:c.952C>G
MANE Select
|
NP_058651.3:p.Pro318Ala
|
|