ENST00000224721.12:c.6337C=
MANE Select
|
ENSP00000224721.9:p.Gln2113=
|
|
ENST00000224721.10:c.6352C=
|
ENSP00000224721.8:p.Gln2118=
|
|
ENST00000622827.4:c.6337C=
|
ENSP00000483211.1:p.Gln2113=
|
|
NM_022124.5:c.6337C=
|
NP_071407.4:p.Gln2113=
|
|
XM_006717940.2:c.6532C=
|
XP_006718003.1:p.Gln2178=
|
|
XM_006717942.2:c.6466C=
|
XP_006718005.1:p.Gln2156=
|
|
XM_011540039.1:c.6529C=
|
XP_011538341.1:p.Gln2177=
|
|
XM_011540040.1:c.6526C=
|
XP_011538342.1:p.Gln2176=
|
|
XM_011540041.1:c.6472C=
|
XP_011538343.1:p.Gln2158=
|
|
XM_011540042.1:c.6532C=
|
XP_011538344.1:p.Gln2178=
|
|
XM_011540043.1:c.6532C=
|
XP_011538345.1:p.Gln2178=
|
|
XM_011540044.1:c.6397C=
|
XP_011538346.1:p.Gln2133=
|
|
XM_011540045.1:c.6532C=
|
XP_011538347.1:p.Gln2178=
|
|
XM_011540046.1:c.5992C=
|
XP_011538348.1:p.Gln1998=
|
|
XM_011540047.1:c.5350C=
|
XP_011538349.1:p.Gln1784=
|
|
XM_011540048.1:c.6532C=
|
XP_011538350.1:p.Gln2178=
|
|
XM_011540049.1:c.6532C=
|
XP_011538351.1:p.Gln2178=
|
|
XM_011540050.1:c.6532C=
|
XP_011538352.1:p.Gln2178=
|
|
XM_011540051.1:c.6532C=
|
XP_011538353.1:p.Gln2178=
|
|
XM_011540052.1:c.2860C=
|
XP_011538354.1:p.Gln954=
|
|
XR_945796.1:n.6775C=
|
|
|
NM_022124.6:c.6337C=
MANE Select
|
NP_071407.4:p.Gln2113=
|
|