ENST00000409959.8:c.4628G>C
MANE Select
|
ENSP00000386787.3:p.Ser1543Thr
|
|
ENST00000240487.5:c.3959G>C
|
ENSP00000240487.5:p.Ser1320Thr
|
|
ENST00000409663.7:c.4625G>C
|
ENSP00000386574.3:p.Ser1542Thr
|
|
ENST00000409959.7:c.4628G>C
|
ENSP00000386787.3:p.Ser1543Thr
|
|
NM_001131007.1:c.4628G>C
|
NP_001124479.1:p.Ser1543Thr
|
|
NM_015196.3:c.4625G>C
|
NP_056011.3:p.Ser1542Thr
|
|
XM_005262871.3:c.2750G>C
|
XP_005262928.2:p.Ser917Thr
|
|
XM_011531780.1:c.4715G>C
|
XP_011530082.1:p.Ser1572Thr
|
|
XM_011531781.1:c.4712G>C
|
XP_011530083.1:p.Ser1571Thr
|
|
XM_011531782.1:c.4685G>C
|
XP_011530084.1:p.Ser1562Thr
|
|
XM_011531783.1:c.4463G>C
|
XP_011530085.1:p.Ser1488Thr
|
|
XM_017007925.1:c.4625G>C
|
XP_016863414.1:p.Ser1542Thr
|
|
XM_017007926.1:c.4622G>C
|
XP_016863415.1:p.Ser1541Thr
|
|
XM_024453956.1:c.4685G>C
|
XP_024309724.1:p.Ser1562Thr
|
|
XM_024453957.1:c.4682G>C
|
XP_024309725.1:p.Ser1561Thr
|
|
XM_024453958.1:c.2750G>C
|
XP_024309726.1:p.Ser917Thr
|
|
NM_001131007.2:c.4628G>C
MANE Select
|
NP_001124479.1:p.Ser1543Thr
|
|
NM_015196.4:c.4625G>C
|
NP_056011.3:p.Ser1542Thr
|
|