ENST00000357166.11:c.329-132G>T
MANE Select
|
ENSP00000349689.6:n.329-132G>T
|
|
ENST00000357166.10:c.329-132G>T
|
ENSP00000349689.6:n.329-132G>T
|
|
ENST00000371064.7:c.329-132G>T
|
ENSP00000360103.3:n.329-132G>T
|
|
ENST00000406492.2:c.329-132G>T
|
ENSP00000383991.2:n.329-132G>T
|
|
ENST00000433917.5:c.208-132G>T
|
|
|
NM_001008222.2:c.329-132G>T
|
NP_001008223.1:n.329-132G>T
|
|
NM_016032.3:c.329-132G>T
|
NP_057116.2:n.329-132G>T
|
|
XM_011531347.1:c.329-132G>T
|
XP_011529649.1:n.329-132G>T
|
|
XM_011531348.1:c.329-132G>T
|
XP_011529650.1:n.329-132G>T
|
|
XM_011531348.3:c.329-132G>T
|
XP_011529650.1:n.329-132G>T
|
|
XR_001755694.2:n.723-132G>T
|
|
|
NM_016032.4:c.329-132G>T
MANE Select
|
NP_057116.2:n.329-132G>T
|
|
NM_001008222.3:c.329-132G>T
|
NP_001008223.1:n.329-132G>T
|
|