ENST00000225964.10:c.4126T>C
MANE Select
|
ENSP00000225964.6:p.Tyr1376His
|
|
ENST00000225964.9:c.4126T>C
|
ENSP00000225964.5:p.Tyr1376His
|
|
ENST00000510710.3:n.1091T>C
|
|
|
NM_000088.3:c.4126T>C , LRG_1t1:c.4126T>C
|
NP_000079.2:p.Tyr1376His
|
|
XM_005257058.3:c.3856T>C
|
XP_005257115.2:p.Tyr1286His
|
|
XM_005257059.3:c.3208T>C
|
XP_005257116.2:p.Tyr1070His
|
|
XM_011524341.1:c.3928T>C
|
XP_011522643.1:p.Tyr1310His
|
|
XM_005257058.4:c.3856T>C
|
XP_005257115.2:p.Tyr1286His
|
|
XM_005257059.4:c.3208T>C
|
XP_005257116.2:p.Tyr1070His
|
|
NM_000088.4:c.4126T>C
MANE Select
|
NP_000079.2:p.Tyr1376His
|
|