|
ENST00000577936.2:c.708A>C
|
ENSP00000462159.2:p.Pro236=
|
|
|
ENST00000579795.6:c.708A>C
MANE Select
|
ENSP00000464645.1:p.Pro236=
|
|
|
ENST00000226247.2:c.708A>C
|
ENSP00000226247.2:p.Pro236=
|
|
|
ENST00000481916.6:c.*1196-72993T>G
|
ENSP00000436369.2:n.*1196-72993T>G
|
|
|
ENST00000579795.5:c.708A>C
|
ENSP00000464645.1:p.Pro236=
|
|
|
NM_003593.2:c.708A>C , LRG_61t1:c.708A>C
|
NP_003584.2:p.Pro236=
|
|
|
XM_005258046.3:c.708A>C
|
XP_005258103.1:p.Pro236=
|
|
|
XM_011525354.1:c.765A>C
|
XP_011523656.1:p.Pro255=
|
|
|
XM_011525355.1:c.762A>C
|
XP_011523657.1:p.Pro254=
|
|
|
XM_011525356.1:c.762A>C
|
XP_011523658.1:p.Pro254=
|
|
|
XM_011525357.1:c.744A>C
|
XP_011523659.1:p.Pro248=
|
|
|
XM_011525358.1:c.711A>C
|
XP_011523660.1:p.Pro237=
|
|
|
XM_011525359.1:c.711A>C
|
XP_011523661.1:p.Pro237=
|
|
|
XM_011525360.1:c.711A>C
|
XP_011523662.1:p.Pro237=
|
|
|
XM_011525361.1:c.708A>C
|
XP_011523663.1:p.Pro236=
|
|
|
XM_011525362.1:c.708A>C
|
XP_011523664.1:p.Pro236=
|
|
|
XM_011525363.1:c.765A>C
|
XP_011523665.1:p.Pro255=
|
|
|
XM_011525364.1:c.243A>C
|
XP_011523666.1:p.Pro81=
|
|
|
XM_011525365.1:c.765A>C
|
XP_011523667.1:p.Pro255=
|
|
|
XM_011525366.1:c.165A>C
|
XP_011523668.1:p.Pro55=
|
|
|
XM_011525367.1:c.150A>C
|
XP_011523669.1:p.Pro50=
|
|
|
XM_011525368.1:c.72A>C
|
XP_011523670.1:p.Pro24=
|
|
|
XM_011525369.1:c.72A>C
|
XP_011523671.1:p.Pro24=
|
|
|
XM_011525370.1:c.72A>C
|
XP_011523672.1:p.Pro24=
|
|
|
XM_011525368.2:c.72A>C
|
XP_011523670.1:p.Pro24=
|
|
|
XM_011525369.2:c.72A>C
|
XP_011523671.1:p.Pro24=
|
|
|
XM_011525370.2:c.72A>C
|
XP_011523672.1:p.Pro24=
|
|
|
XM_017025228.1:c.708A>C
|
XP_016880717.1:p.Pro236=
|
|
|
XM_017025229.1:c.711A>C
|
XP_016880718.1:p.Pro237=
|
|
|
XM_017025230.1:c.711A>C
|
XP_016880719.1:p.Pro237=
|
|
|
XM_017025231.1:c.711A>C
|
XP_016880720.1:p.Pro237=
|
|
|
NM_001369369.1:c.708A>C
MANE Select
|
NP_001356298.1:p.Pro236=
|
|
|
NM_003593.3:c.708A>C
|
NP_003584.2:p.Pro236=
|
|
