ENST00000224721.12:c.6049G=
MANE Select
|
ENSP00000224721.9:p.Gly2017=
|
|
ENST00000224721.10:c.6064G=
|
ENSP00000224721.8:p.Gly2022=
|
|
ENST00000622827.4:c.6049G=
|
ENSP00000483211.1:p.Gly2017=
|
|
NM_022124.5:c.6049G=
|
NP_071407.4:p.Gly2017=
|
|
XM_006717940.2:c.6244G=
|
XP_006718003.1:p.Gly2082=
|
|
XM_006717942.2:c.6178G=
|
XP_006718005.1:p.Gly2060=
|
|
XM_011540039.1:c.6241G=
|
XP_011538341.1:p.Gly2081=
|
|
XM_011540040.1:c.6238G=
|
XP_011538342.1:p.Gly2080=
|
|
XM_011540041.1:c.6184G=
|
XP_011538343.1:p.Gly2062=
|
|
XM_011540042.1:c.6244G=
|
XP_011538344.1:p.Gly2082=
|
|
XM_011540043.1:c.6244G=
|
XP_011538345.1:p.Gly2082=
|
|
XM_011540044.1:c.6109G=
|
XP_011538346.1:p.Gly2037=
|
|
XM_011540045.1:c.6244G=
|
XP_011538347.1:p.Gly2082=
|
|
XM_011540046.1:c.5704G=
|
XP_011538348.1:p.Gly1902=
|
|
XM_011540047.1:c.5062G=
|
XP_011538349.1:p.Gly1688=
|
|
XM_011540048.1:c.6244G=
|
XP_011538350.1:p.Gly2082=
|
|
XM_011540049.1:c.6244G=
|
XP_011538351.1:p.Gly2082=
|
|
XM_011540050.1:c.6244G=
|
XP_011538352.1:p.Gly2082=
|
|
XM_011540051.1:c.6244G=
|
XP_011538353.1:p.Gly2082=
|
|
XM_011540052.1:c.2572G=
|
XP_011538354.1:p.Gly858=
|
|
XR_945796.1:n.6487G=
|
|
|
NM_022124.6:c.6049G=
MANE Select
|
NP_071407.4:p.Gly2017=
|
|