ENST00000332981.11:c.1357G>A
MANE Select
|
ENSP00000329127.5:p.Glu453Lys
|
|
ENST00000332981.10:c.1357G>A
|
ENSP00000329127.5:p.Glu453Lys
|
|
ENST00000640011.1:c.46G>A
|
ENSP00000491586.1:p.Glu16Lys
|
|
ENST00000332981.9:c.1357G>A
|
ENSP00000329127.5:p.Glu453Lys
|
|
ENST00000536400.5:n.158G>A
|
|
|
ENST00000555082.5:c.874G>A
|
ENSP00000450981.1:p.Glu292Lys
|
|
ENST00000555185.5:c.61G>A
|
ENSP00000451871.1:p.Glu21Lys
|
|
ENST00000555233.5:n.371G>A
|
|
|
NM_006255.4:c.1357G>A
|
NP_006246.2:p.Glu453Lys
|
|
XM_011536954.1:c.1120G>A
|
XP_011535256.1:p.Glu374Lys
|
|
XM_011536955.1:c.1117G>A
|
XP_011535257.1:p.Glu373Lys
|
|
XM_011536956.1:c.1357G>A
|
XP_011535258.1:p.Glu453Lys
|
|
XM_011536957.1:c.1357G>A
|
XP_011535259.1:p.Glu453Lys
|
|
XM_011536954.3:c.1120G>A
|
XP_011535256.1:p.Glu374Lys
|
|
XM_017021458.1:c.874G>A
|
XP_016876947.1:p.Glu292Lys
|
|
XM_024449661.1:c.874G>A
|
XP_024305429.1:p.Glu292Lys
|
|
XM_024449662.1:c.874G>A
|
XP_024305430.1:p.Glu292Lys
|
|
NM_006255.5:c.1357G>A
MANE Select
|
NP_006246.2:p.Glu453Lys
|
|