|
NM_001329998.2:c.2981G>A
MANE Select
|
NP_001316927.1:p.Arg994His
|
|
ENST00000645898.2:c.2981G>A
MANE Select
|
ENSP00000494480.1:p.Arg994His
|
|
NM_001329998.1:c.2981G>A
|
NP_001316927.1:p.Arg994His
|
|
NM_014831.2:c.2849G>A
|
NP_055646.2:p.Arg950His
|
|
NM_014831.3:c.2849G>A
|
NP_055646.2:p.Arg950His
|
|
ENST00000429976.5:c.2849G>A
|
ENSP00000416168.2:p.Arg950His
|
|
ENST00000643881.1:c.892G>A
|
|
|
ENST00000646897.1:c.2957G>A
|
ENSP00000496771.1:p.Arg986His
|
|
XM_006713432.2:c.2981G>A
|
XP_006713495.1:p.Arg994His
|
|
XM_011534289.1:c.2984G>A
|
XP_011532591.1:p.Arg995His
|
|
XM_011534289.2:c.2984G>A
|
XP_011532591.1:p.Arg995His
|
|
XM_011534290.1:c.2957G>A
|
XP_011532592.1:p.Arg986His
|
|
XM_011534291.1:c.2957G>A
|
XP_011532593.1:p.Arg986His
|
|
XM_011534292.1:c.2813G>A
|
XP_011532594.1:p.Arg938His
|
|
XM_011534293.1:c.2315G>A
|
XP_011532595.1:p.Arg772His
|
|
XM_011534294.1:c.2984G>A
|
XP_011532596.1:p.Arg995His
|
|
XM_017007570.1:c.2882G>A
|
XP_016863059.1:p.Arg961His
|
|
XM_017007571.1:c.3053G>A
|
XP_016863060.1:p.Arg1018His
|
|
XM_017007572.1:c.2957G>A
|
XP_016863061.1:p.Arg986His
|
|
XM_017007573.1:c.3053G>A
|
XP_016863062.1:p.Arg1018His
|
|
XR_001740389.1:n.3068G>A
|
|
|
XR_001740390.1:n.3068G>A
|
|
|
XR_940526.1:n.4022G>A
|
|