ENST00000298910.12:c.6039A>G
MANE Select
|
ENSP00000298910.7:p.Ala2013=
|
|
ENST00000679360.1:c.*4948A>G
|
ENSP00000505368.1:n.*4948A>G
|
|
ENST00000679532.1:c.1813A>G
|
|
|
ENST00000680018.1:c.1484A>G
|
ENSP00000505347.1:n.1484A>G
|
|
ENST00000680422.1:c.1684A>G
|
|
|
ENST00000680425.1:c.1206A>G
|
ENSP00000506459.1:n.1206A>G
|
|
ENST00000680453.1:c.1496A>G
|
|
|
ENST00000680790.1:c.5784A>G
|
ENSP00000505335.1:p.Ala1928=
|
|
ENST00000681136.1:n.2023A>G
|
|
|
ENST00000681696.1:c.1722A>G
|
ENSP00000505871.1:p.Ala574=
|
|
ENST00000298910.11:c.6039A>G
|
ENSP00000298910.7:p.Ala2013=
|
|
ENST00000430804.5:c.3335A>G
|
|
|
ENST00000479187.5:n.2720A>G
|
|
|
NM_198578.3:c.6039A>G
|
NP_940980.3:p.Ala2013=
|
|
XM_005268629.2:c.6039A>G
|
XP_005268686.1:p.Ala2013=
|
|
XM_011537877.1:c.6039A>G
|
XP_011536179.1:p.Ala2013=
|
|
XM_011537878.1:c.6039A>G
|
XP_011536180.1:p.Ala2013=
|
|
XM_011537879.1:c.4836A>G
|
XP_011536181.1:p.Ala1612=
|
|
XM_005268629.4:c.6039A>G
|
XP_005268686.1:p.Ala2013=
|
|
XM_011537877.3:c.6039A>G
|
XP_011536179.1:p.Ala2013=
|
|
XM_017018787.1:c.2955A>G
|
XP_016874276.1:p.Ala985=
|
|
XM_017018788.2:c.2301A>G
|
XP_016874277.1:p.Ala767=
|
|
XM_024448833.1:c.4836A>G
|
XP_024304601.1:p.Ala1612=
|
|
NM_198578.4:c.6039A>G
MANE Select
|
NP_940980.4:p.Ala2013=
|
|