|
NM_003036.4:c.1339G>A
MANE Select
|
NP_003027.1:p.Ala447Thr
|
|
ENST00000378536.5:c.1339G>A
MANE Select
|
ENSP00000367797.4:p.Ala447Thr
|
|
NM_003036.3:c.1339G>A
|
NP_003027.1:p.Ala447Thr
|
|
ENST00000378536.4:c.1339G>A
|
ENSP00000367797.4:p.Ala447Thr
|
|
ENST00000507179.1:n.322G>A
|
|
|
XM_005244775.2:c.1339G>A
|
XP_005244832.1:p.Ala447Thr
|
|
XM_005244775.3:c.1339G>A
|
XP_005244832.1:p.Ala447Thr
|
|
XM_005244776.3:c.469G>A
|
XP_005244833.1:p.Ala157Thr
|
|
XM_005244776.4:c.469G>A
|
XP_005244833.1:p.Ala157Thr
|
|
XM_017002128.1:c.847G>A
|
XP_016857617.1:p.Ala283Thr
|