ENST00000225964.10:c.4348C>G
MANE Select
|
ENSP00000225964.6:p.Pro1450Ala
|
|
ENST00000225964.9:c.4348C>G
|
ENSP00000225964.5:p.Pro1450Ala
|
|
NM_000088.3:c.4348C>G , LRG_1t1:c.4348C>G
|
NP_000079.2:p.Pro1450Ala
|
|
XM_005257058.3:c.4078C>G
|
XP_005257115.2:p.Pro1360Ala
|
|
XM_005257059.3:c.3430C>G
|
XP_005257116.2:p.Pro1144Ala
|
|
XM_011524341.1:c.4150C>G
|
XP_011522643.1:p.Pro1384Ala
|
|
XM_005257058.4:c.4078C>G
|
XP_005257115.2:p.Pro1360Ala
|
|
XM_005257059.4:c.3430C>G
|
XP_005257116.2:p.Pro1144Ala
|
|
NM_000088.4:c.4348C>G
MANE Select
|
NP_000079.2:p.Pro1450Ala
|
|