ENST00000378154.3:c.2695G>T
|
ENSP00000367396.2:p.Ala899Ser
|
|
ENST00000378158.6:c.2692G>T
|
ENSP00000367400.2:p.Ala898Ser
|
|
ENST00000378163.7:c.2746G>T
MANE Select
|
ENSP00000367405.1:p.Ala916Ser
|
|
ENST00000378166.9:c.2644G>T
|
ENSP00000367408.5:p.Ala882Ser
|
|
ENST00000378168.8:c.2749G>T
|
ENSP00000367410.4:p.Ala917Ser
|
|
ENST00000378179.9:c.1366G>T
|
ENSP00000367421.4:p.Ala456Ser
|
|
ENST00000421587.8:c.2677G>T
|
ENSP00000400526.4:p.Ala893Ser
|
|
ENST00000442742.7:c.2608G>T
|
ENSP00000398007.3:p.Ala870Ser
|
|
ENST00000642499.1:n.1525G>T
|
|
|
ENST00000642641.1:n.905G>T
|
|
|
ENST00000643733.1:c.545G>T
|
|
|
ENST00000644219.1:c.2728G>T
|
ENSP00000495357.1:p.Ala910Ser
|
|
ENST00000644347.1:c.2659G>T
|
ENSP00000494183.1:p.Ala887Ser
|
|
ENST00000645566.1:c.2731G>T
|
ENSP00000494788.1:p.Ala911Ser
|
|
ENST00000645937.2:n.2977G>T
|
|
|
ENST00000645986.2:c.2833G>T
|
ENSP00000494409.2:p.Ala945Ser
|
|
ENST00000646087.2:c.2068G>T
|
ENSP00000495510.2:p.Ala690Ser
|
|
ENST00000646120.2:c.2662G>T
|
ENSP00000495291.2:p.Ala888Ser
|
|
ENST00000675354.1:c.2680G>T
|
ENSP00000502315.1:p.Ala894Ser
|
|
ENST00000378158.5:c.2695G>T
|
ENSP00000367400.1:p.Ala899Ser
|
|
ENST00000378163.5:c.2746G>T
|
ENSP00000367405.1:p.Ala916Ser
|
|
ENST00000378166.8:c.2731G>T
|
ENSP00000367408.4:p.Ala911Ser
|
|
ENST00000378168.6:c.1111G>T
|
ENSP00000367410.2:p.Ala371Ser
|
|
ENST00000378179.7:c.1522G>T
|
ENSP00000367421.3:p.Ala508Ser
|
|
ENST00000421587.6:c.2659G>T
|
ENSP00000400526.2:p.Ala887Ser
|
|
ENST00000442742.6:c.2662G>T
|
ENSP00000398007.2:p.Ala888Ser
|
|
NM_001126054.2:c.2662G>T
|
NP_001119526.1:p.Ala888Ser
|
|
NM_001126055.2:c.2659G>T
|
NP_001119527.1:p.Ala887Ser
|
|
NM_003688.3:c.2731G>T
|
NP_003679.2:p.Ala911Ser
|
|
XM_005272686.3:c.2728G>T
|
XP_005272743.1:p.Ala910Ser
|
|
XM_006724566.2:c.2623G>T
|
XP_006724629.1:p.Ala875Ser
|
|
XM_011543993.1:c.2746G>T
|
XP_011542295.1:p.Ala916Ser
|
|
XM_011543994.1:c.2710G>T
|
XP_011542296.1:p.Ala904Ser
|
|
XM_011543995.1:c.2677G>T
|
XP_011542297.1:p.Ala893Ser
|
|
XM_011543996.1:c.2641G>T
|
XP_011542298.1:p.Ala881Ser
|
|
XM_011543997.1:c.2173G>T
|
XP_011542299.1:p.Ala725Ser
|
|
XM_005272686.4:c.2728G>T
|
XP_005272743.1:p.Ala910Ser
|
|
XM_006724566.3:c.2623G>T
|
XP_006724629.1:p.Ala875Ser
|
|
XM_011543993.2:c.2746G>T
|
XP_011542295.1:p.Ala916Ser
|
|
XM_011543994.2:c.2710G>T
|
XP_011542296.1:p.Ala904Ser
|
|
XM_011543995.2:c.2677G>T
|
XP_011542297.1:p.Ala893Ser
|
|
XM_011543996.2:c.2641G>T
|
XP_011542298.1:p.Ala881Ser
|
|
XM_011543997.3:c.2173G>T
|
XP_011542299.1:p.Ala725Ser
|
|
XM_024452473.1:c.2068G>T
|
XP_024308241.1:p.Ala690Ser
|
|
NM_001367721.1:c.2746G>T
MANE Select
|
NP_001354650.1:p.Ala916Ser
|
|