|
NM_003036.4:c.1528G>T
MANE Select
|
NP_003027.1:p.Ala510Ser
|
|
ENST00000378536.5:c.1528G>T
MANE Select
|
ENSP00000367797.4:p.Ala510Ser
|
|
NM_003036.3:c.1528G>T
|
NP_003027.1:p.Ala510Ser
|
|
ENST00000378536.4:c.1528G>T
|
ENSP00000367797.4:p.Ala510Ser
|
|
ENST00000507179.1:n.517G>T
|
|
|
XM_005244775.2:c.1534G>T
|
XP_005244832.1:p.Ala512Ser
|
|
XM_005244775.3:c.1534G>T
|
XP_005244832.1:p.Ala512Ser
|
|
XM_005244776.3:c.664G>T
|
XP_005244833.1:p.Ala222Ser
|
|
XM_005244776.4:c.664G>T
|
XP_005244833.1:p.Ala222Ser
|
|
XM_017002128.1:c.1042G>T
|
XP_016857617.1:p.Ala348Ser
|