ENST00000224721.12:c.6296G>T
MANE Select
|
ENSP00000224721.9:p.Gly2099Val
|
|
ENST00000224721.10:c.6311G>T
|
ENSP00000224721.8:p.Gly2104Val
|
|
ENST00000622827.4:c.6296G>T
|
ENSP00000483211.1:p.Gly2099Val
|
|
NM_022124.5:c.6296G>T
|
NP_071407.4:p.Gly2099Val
|
|
XM_006717940.2:c.6491G>T
|
XP_006718003.1:p.Gly2164Val
|
|
XM_006717942.2:c.6425G>T
|
XP_006718005.1:p.Gly2142Val
|
|
XM_011540039.1:c.6488G>T
|
XP_011538341.1:p.Gly2163Val
|
|
XM_011540040.1:c.6485G>T
|
XP_011538342.1:p.Gly2162Val
|
|
XM_011540041.1:c.6431G>T
|
XP_011538343.1:p.Gly2144Val
|
|
XM_011540042.1:c.6491G>T
|
XP_011538344.1:p.Gly2164Val
|
|
XM_011540043.1:c.6491G>T
|
XP_011538345.1:p.Gly2164Val
|
|
XM_011540044.1:c.6356G>T
|
XP_011538346.1:p.Gly2119Val
|
|
XM_011540045.1:c.6491G>T
|
XP_011538347.1:p.Gly2164Val
|
|
XM_011540046.1:c.5951G>T
|
XP_011538348.1:p.Gly1984Val
|
|
XM_011540047.1:c.5309G>T
|
XP_011538349.1:p.Gly1770Val
|
|
XM_011540048.1:c.6491G>T
|
XP_011538350.1:p.Gly2164Val
|
|
XM_011540049.1:c.6491G>T
|
XP_011538351.1:p.Gly2164Val
|
|
XM_011540050.1:c.6491G>T
|
XP_011538352.1:p.Gly2164Val
|
|
XM_011540051.1:c.6491G>T
|
XP_011538353.1:p.Gly2164Val
|
|
XM_011540052.1:c.2819G>T
|
XP_011538354.1:p.Gly940Val
|
|
XR_945796.1:n.6734G>T
|
|
|
NM_022124.6:c.6296G>T
MANE Select
|
NP_071407.4:p.Gly2099Val
|
|