ENST00000649448.1:c.779C>T
|
ENSP00000497165.1:p.Ala260Val
|
|
ENST00000650372.1:c.2462C>T
MANE Select
|
ENSP00000497931.1:p.Ala821Val
|
|
ENST00000263817.6:c.2462C>T
|
ENSP00000263817.6:p.Ala821Val
|
|
ENST00000439188.1:c.1151C>T
|
ENSP00000416058.1:n.1151C>T
|
|
NM_003742.2:c.2462C>T
|
NP_003733.2:p.Ala821Val
|
|
XM_006712817.2:c.2504C>T
|
XP_006712880.1:p.Ala835Val
|
|
XM_011512077.1:c.2564C>T
|
XP_011510379.1:p.Ala855Val
|
|
XM_011512078.1:c.2564C>T
|
XP_011510380.1:p.Ala855Val
|
|
XM_011512079.1:c.2564C>T
|
XP_011510381.1:p.Ala855Val
|
|
XM_011512080.1:c.2564C>T
|
XP_011510382.1:p.Ala855Val
|
|
XM_011512081.1:c.788C>T
|
XP_011510383.1:p.Ala263Val
|
|
NM_003742.4:c.2462C>T
MANE Select
|
NP_003733.2:p.Ala821Val
|
|
XM_006712817.3:c.2504C>T
|
XP_006712880.1:p.Ala835Val
|
|
XM_011512077.2:c.2564C>T
|
XP_011510379.1:p.Ala855Val
|
|
XM_011512078.2:c.2564C>T
|
XP_011510380.1:p.Ala855Val
|
|
XM_011512080.2:c.2564C>T
|
XP_011510382.1:p.Ala855Val
|
|
XM_011512081.2:c.788C>T
|
XP_011510383.1:p.Ala263Val
|
|
XM_017005165.1:c.2564C>T
|
XP_016860654.1:p.Ala855Val
|
|
XM_017005166.1:c.1793C>T
|
XP_016860655.1:p.Ala598Val
|
|
XM_017005167.1:c.1247C>T
|
XP_016860656.1:p.Ala416Val
|
|