ENST00000234071.8:c.1293C>A
MANE Select
|
ENSP00000234071.4:p.Asn431Lys
|
|
ENST00000234071.7:c.1293C>A
|
ENSP00000234071.3:p.Asn431Lys
|
|
ENST00000402125.2:c.617C>A
|
|
|
ENST00000409048.1:c.1395C>A
|
ENSP00000386679.1:p.Asn465Lys
|
|
NM_000312.3:c.1293C>A , LRG_599t1:c.1293C>A
|
NP_000303.1:p.Asn431Lys
|
|
XM_005263715.3:c.1476C>A
|
XP_005263772.1:p.Asn492Lys
|
|
XM_005263716.3:c.1458C>A
|
XP_005263773.1:p.Asn486Lys
|
|
XM_005263717.3:c.1356C>A
|
XP_005263774.1:p.Asn452Lys
|
|
XR_923313.1:n.1332-589G>T
|
|
|
XM_005263717.4:c.1356C>A
|
XP_005263774.1:p.Asn452Lys
|
|
XM_017004505.1:c.1536C>A
|
XP_016859994.1:p.Asn512Lys
|
|
XM_024453002.1:c.1638C>A
|
XP_024308770.1:p.Asn546Lys
|
|
XM_024453003.1:c.1578C>A
|
XP_024308771.1:p.Asn526Lys
|
|
XM_024453004.1:c.1476C>A
|
XP_024308772.1:p.Asn492Lys
|
|
XM_024453005.1:c.1458C>A
|
XP_024308773.1:p.Asn486Lys
|
|
XM_024453006.1:c.1395C>A
|
XP_024308774.1:p.Asn465Lys
|
|
XR_001739705.1:n.3607-589G>T
|
|
|
XR_923313.2:n.4043-589G>T
|
|
|
NM_000312.4:c.1293C>A
MANE Select
|
NP_000303.1:p.Asn431Lys
|
|
NM_001375602.1:c.1476C>A
|
NP_001362531.1:p.Asn492Lys
|
|
NM_001375603.1:c.1458C>A
|
NP_001362532.1:p.Asn486Lys
|
|
NM_001375604.1:c.1356C>A
|
NP_001362533.1:p.Asn452Lys
|
|
NM_001375605.1:c.1395C>A
|
NP_001362534.1:p.Asn465Lys
|
|
NM_001375606.1:c.1461C>A
|
NP_001362535.1:p.Asn487Lys
|
|
NM_001375607.1:c.1479C>A
|
NP_001362536.1:p.Asn493Lys
|
|
NM_001375608.1:c.1236C>A
|
NP_001362537.1:p.Asn412Lys
|
|
NM_001375609.1:c.1269C>A
|
NP_001362538.1:p.Asn423Lys
|
|
NM_001375610.1:c.1287C>A
|
NP_001362539.1:p.Asn429Lys
|
|
NM_001375611.1:c.1293C>A
|
NP_001362540.1:p.Asn431Lys
|
|
NM_001375613.1:c.1293C>A
|
NP_001362542.1:p.Asn431Lys
|
|