ENST00000225964.10:c.1399G>T
MANE Select
|
ENSP00000225964.6:p.Gly467Ter
|
|
ENST00000225964.9:c.1399G>T
|
ENSP00000225964.5:p.Gly467Ter
|
|
ENST00000471344.1:n.343G>T
|
|
|
NM_000088.3:c.1399G>T , LRG_1t1:c.1399G>T
|
NP_000079.2:p.Gly467Ter
|
|
XM_005257058.3:c.1399G>T
|
XP_005257115.2:p.Gly467Ter
|
|
XM_005257059.3:c.957+1531G>T
|
XP_005257116.2:n.957+1531G>T
|
|
XM_011524341.1:c.1201G>T
|
XP_011522643.1:p.Gly401Ter
|
|
XM_005257058.4:c.1399G>T
|
XP_005257115.2:p.Gly467Ter
|
|
XM_005257059.4:c.957+1531G>T
|
XP_005257116.2:n.957+1531G>T
|
|
NM_000088.4:c.1399G>T
MANE Select
|
NP_000079.2:p.Gly467Ter
|
|