ENST00000234071.8:c.1064A>C
MANE Select
|
ENSP00000234071.4:p.Asn355Thr
|
|
ENST00000234071.7:c.1064A>C
|
ENSP00000234071.3:p.Asn355Thr
|
|
ENST00000402125.2:c.388A>C
|
|
|
ENST00000409048.1:c.1166A>C
|
ENSP00000386679.1:p.Asn389Thr
|
|
NM_000312.3:c.1064A>C , LRG_599t1:c.1064A>C
|
NP_000303.1:p.Asn355Thr
|
|
XM_005263715.3:c.1247A>C
|
XP_005263772.1:p.Asn416Thr
|
|
XM_005263716.3:c.1229A>C
|
XP_005263773.1:p.Asn410Thr
|
|
XM_005263717.3:c.1127A>C
|
XP_005263774.1:p.Asn376Thr
|
|
XR_923313.1:n.1332-360T>G
|
|
|
XM_005263717.4:c.1127A>C
|
XP_005263774.1:p.Asn376Thr
|
|
XM_017004505.1:c.1307A>C
|
XP_016859994.1:p.Asn436Thr
|
|
XM_024453002.1:c.1409A>C
|
XP_024308770.1:p.Asn470Thr
|
|
XM_024453003.1:c.1349A>C
|
XP_024308771.1:p.Asn450Thr
|
|
XM_024453004.1:c.1247A>C
|
XP_024308772.1:p.Asn416Thr
|
|
XM_024453005.1:c.1229A>C
|
XP_024308773.1:p.Asn410Thr
|
|
XM_024453006.1:c.1166A>C
|
XP_024308774.1:p.Asn389Thr
|
|
XR_001739705.1:n.3607-360T>G
|
|
|
XR_923313.2:n.4043-360T>G
|
|
|
NM_000312.4:c.1064A>C
MANE Select
|
NP_000303.1:p.Asn355Thr
|
|
NM_001375602.1:c.1247A>C
|
NP_001362531.1:p.Asn416Thr
|
|
NM_001375603.1:c.1229A>C
|
NP_001362532.1:p.Asn410Thr
|
|
NM_001375604.1:c.1127A>C
|
NP_001362533.1:p.Asn376Thr
|
|
NM_001375605.1:c.1166A>C
|
NP_001362534.1:p.Asn389Thr
|
|
NM_001375606.1:c.1232A>C
|
NP_001362535.1:p.Asn411Thr
|
|
NM_001375607.1:c.1250A>C
|
NP_001362536.1:p.Asn417Thr
|
|
NM_001375608.1:c.1007A>C
|
NP_001362537.1:p.Asn336Thr
|
|
NM_001375609.1:c.1040A>C
|
NP_001362538.1:p.Asn347Thr
|
|
NM_001375610.1:c.1058A>C
|
NP_001362539.1:p.Asn353Thr
|
|
NM_001375611.1:c.1064A>C
|
NP_001362540.1:p.Asn355Thr
|
|
NM_001375613.1:c.1064A>C
|
NP_001362542.1:p.Asn355Thr
|
|