ENST00000355943.8:c.926T>A
MANE Select
|
ENSP00000348211.3:p.Met309Lys
|
|
ENST00000355943.7:c.926T>A
|
ENSP00000348211.3:p.Met309Lys
|
|
ENST00000447245.6:c.683T>A
|
ENSP00000399717.2:p.Met228Lys
|
|
ENST00000502462.6:n.1242T>A
|
|
|
ENST00000504098.1:c.488T>A
|
ENSP00000425708.1:p.Met163Lys
|
|
ENST00000509432.1:c.287T>A
|
ENSP00000426604.1:p.Met96Lys
|
|
ENST00000513706.2:n.2526T>A
|
|
|
ENST00000513807.5:c.440T>A
|
ENSP00000421134.1:p.Met147Lys
|
|
NM_001303249.1:c.683T>A
|
NP_001290178.1:p.Met228Lys
|
|
NM_001303250.1:c.653T>A
|
NP_001290179.1:p.Met218Lys
|
|
NM_138773.2:c.926T>A
|
NP_620128.1:p.Met309Lys
|
|
NM_001303249.2:c.683T>A
|
NP_001290178.1:p.Met228Lys
|
|
NM_001303250.2:c.653T>A
|
NP_001290179.1:p.Met218Lys
|
|
NM_138773.3:c.926T>A
|
NP_620128.1:p.Met309Lys
|
|
NR_138151.1:n.1200T>A
|
|
|
NM_138773.4:c.926T>A
MANE Select
|
NP_620128.1:p.Met309Lys
|
|
NM_001303249.3:c.683T>A
|
NP_001290178.1:p.Met228Lys
|
|
NM_001303250.3:c.653T>A
|
NP_001290179.1:p.Met218Lys
|
|
NR_138151.2:n.1165T>A
|
|
|