ENST00000330498.4:c.1367T>C
MANE Select
|
ENSP00000327943.3:p.Ile456Thr
|
|
ENST00000330498.3:c.1367T>C
|
ENSP00000327943.3:p.Ile456Thr
|
|
ENST00000419665.6:c.1130-157T>C
|
ENSP00000410601.2:n.1130-157T>C
|
|
ENST00000568188.1:n.738T>C
|
|
|
ENST00000568891.1:n.282-157T>C
|
|
|
NM_003041.3:c.1367T>C
|
NP_003032.1:p.Ile456Thr
|
|
NR_130783.1:n.1149-157T>C
|
|
|
XM_006721072.2:c.1388T>C
|
XP_006721135.2:p.Ile463Thr
|
|
XM_006721073.2:c.1302-157T>C
|
XP_006721136.2:n.1302-157T>C
|
|
XM_006721072.4:c.1388T>C
|
XP_006721135.2:p.Ile463Thr
|
|
XM_024450402.1:c.1151-157T>C
|
XP_024306170.1:n.1151-157T>C
|
|
NM_003041.4:c.1367T>C
MANE Select
|
NP_003032.1:p.Ile456Thr
|
|
NR_130783.2:n.1144-157T>C
|
|
|