ENST00000378154.3:c.2391G=
|
ENSP00000367396.2:p.Ala797=
|
|
ENST00000378158.6:c.2388G=
|
ENSP00000367400.2:p.Ala796=
|
|
ENST00000378163.7:c.2442G=
MANE Select
|
ENSP00000367405.1:p.Ala814=
|
|
ENST00000378166.9:c.2340G=
|
ENSP00000367408.5:p.Ala780=
|
|
ENST00000378168.8:c.2445G=
|
ENSP00000367410.4:p.Ala815=
|
|
ENST00000378179.9:c.1062G=
|
ENSP00000367421.4:p.Ala354=
|
|
ENST00000421587.8:c.2373G=
|
ENSP00000400526.4:p.Ala791=
|
|
ENST00000442742.7:c.2304G=
|
ENSP00000398007.3:p.Ala768=
|
|
ENST00000642499.1:n.1221G=
|
|
|
ENST00000643733.1:c.214G=
|
|
|
ENST00000644219.1:c.2424G=
|
ENSP00000495357.1:p.Ala808=
|
|
ENST00000644347.1:c.2355G=
|
ENSP00000494183.1:p.Ala785=
|
|
ENST00000645566.1:c.2427G=
|
ENSP00000494788.1:p.Ala809=
|
|
ENST00000645937.2:n.2673G=
|
|
|
ENST00000645986.2:c.2409G=
|
ENSP00000494409.2:p.Ala803=
|
|
ENST00000646087.2:c.1764G=
|
ENSP00000495510.2:p.Ala588=
|
|
ENST00000646120.2:c.2358G=
|
ENSP00000495291.2:p.Ala786=
|
|
ENST00000675354.1:c.2376G=
|
ENSP00000502315.1:p.Ala792=
|
|
ENST00000378158.5:c.2391G=
|
ENSP00000367400.1:p.Ala797=
|
|
ENST00000378163.5:c.2442G=
|
ENSP00000367405.1:p.Ala814=
|
|
ENST00000378166.8:c.2427G=
|
ENSP00000367408.4:p.Ala809=
|
|
ENST00000378168.6:c.807G=
|
ENSP00000367410.2:p.Ala269=
|
|
ENST00000378179.7:c.1218G=
|
ENSP00000367421.3:p.Ala406=
|
|
ENST00000421587.6:c.2355G=
|
ENSP00000400526.2:p.Ala785=
|
|
ENST00000442742.6:c.2358G=
|
ENSP00000398007.2:p.Ala786=
|
|
NM_001126054.2:c.2358G=
|
NP_001119526.1:p.Ala786=
|
|
NM_001126055.2:c.2355G=
|
NP_001119527.1:p.Ala785=
|
|
NM_003688.3:c.2427G=
|
NP_003679.2:p.Ala809=
|
|
XM_005272686.3:c.2424G=
|
XP_005272743.1:p.Ala808=
|
|
XM_006724566.2:c.2319G=
|
XP_006724629.1:p.Ala773=
|
|
XM_011543993.1:c.2442G=
|
XP_011542295.1:p.Ala814=
|
|
XM_011543994.1:c.2406G=
|
XP_011542296.1:p.Ala802=
|
|
XM_011543995.1:c.2373G=
|
XP_011542297.1:p.Ala791=
|
|
XM_011543996.1:c.2337G=
|
XP_011542298.1:p.Ala779=
|
|
XM_011543997.1:c.1869G=
|
XP_011542299.1:p.Ala623=
|
|
XM_005272686.4:c.2424G=
|
XP_005272743.1:p.Ala808=
|
|
XM_006724566.3:c.2319G=
|
XP_006724629.1:p.Ala773=
|
|
XM_011543993.2:c.2442G=
|
XP_011542295.1:p.Ala814=
|
|
XM_011543994.2:c.2406G=
|
XP_011542296.1:p.Ala802=
|
|
XM_011543995.2:c.2373G=
|
XP_011542297.1:p.Ala791=
|
|
XM_011543996.2:c.2337G=
|
XP_011542298.1:p.Ala779=
|
|
XM_011543997.3:c.1869G=
|
XP_011542299.1:p.Ala623=
|
|
XM_024452473.1:c.1764G=
|
XP_024308241.1:p.Ala588=
|
|
NM_001367721.1:c.2442G=
MANE Select
|
NP_001354650.1:p.Ala814=
|
|