ENST00000225964.10:c.4395A>C
MANE Select
|
ENSP00000225964.6:p.Ter1465Tyr
|
|
ENST00000225964.9:c.4395A>C
|
ENSP00000225964.5:p.Ter1465Tyr
|
|
NM_000088.3:c.4395A>C , LRG_1t1:c.4395A>C
|
NP_000079.2:p.Ter1465Tyr
|
|
XM_005257058.3:c.4125A>C
|
XP_005257115.2:p.Ter1375Tyr
|
|
XM_005257059.3:c.3477A>C
|
XP_005257116.2:p.Ter1159Tyr
|
|
XM_011524341.1:c.4197A>C
|
XP_011522643.1:p.Ter1399Tyr
|
|
XM_005257058.4:c.4125A>C
|
XP_005257115.2:p.Ter1375Tyr
|
|
XM_005257059.4:c.3477A>C
|
XP_005257116.2:p.Ter1159Tyr
|
|
NM_000088.4:c.4395A>C
MANE Select
|
NP_000079.2:p.Ter1465Tyr
|
|