ENST00000225964.10:c.3160C>G
MANE Select
|
ENSP00000225964.6:p.Pro1054Ala
|
|
ENST00000225964.9:c.3160C>G
|
ENSP00000225964.5:p.Pro1054Ala
|
|
ENST00000511732.1:n.104C>G
|
|
|
NM_000088.3:c.3160C>G , LRG_1t1:c.3160C>G
|
NP_000079.2:p.Pro1054Ala
|
|
XM_005257058.3:c.2890C>G
|
XP_005257115.2:p.Pro964Ala
|
|
XM_005257059.3:c.2242C>G
|
XP_005257116.2:p.Pro748Ala
|
|
XM_011524341.1:c.2962C>G
|
XP_011522643.1:p.Pro988Ala
|
|
XM_005257058.4:c.2890C>G
|
XP_005257115.2:p.Pro964Ala
|
|
XM_005257059.4:c.2242C>G
|
XP_005257116.2:p.Pro748Ala
|
|
NM_000088.4:c.3160C>G
MANE Select
|
NP_000079.2:p.Pro1054Ala
|
|