ENST00000224140.6:c.4356A>G
MANE Select
|
ENSP00000224140.5:p.Pro1452=
|
|
ENST00000224140.5:c.4356A>G
|
ENSP00000224140.5:p.Pro1452=
|
|
NM_015046.5:c.4356A>G , LRG_268t1:c.4356A>G
|
NP_055861.3:p.Pro1452=
|
|
XM_005272171.1:c.4356A>G
|
XP_005272228.1:p.Pro1452=
|
|
XM_005272172.1:c.4356A>G
|
XP_005272229.1:p.Pro1452=
|
|
XM_005272173.1:c.4356A>G
|
XP_005272230.1:p.Pro1452=
|
|
XM_011518404.1:c.4356A>G
|
XP_011516706.1:p.Pro1452=
|
|
XM_011518405.1:c.4356A>G
|
XP_011516707.1:p.Pro1452=
|
|
XM_011518406.1:c.4356A>G
|
XP_011516708.1:p.Pro1452=
|
|
XM_011518407.1:c.4356A>G
|
XP_011516709.1:p.Pro1452=
|
|
XM_011518408.1:c.4356A>G
|
XP_011516710.1:p.Pro1452=
|
|
XR_929739.1:n.4540A>G
|
|
|
NM_001351527.1:c.4356A>G
|
NP_001338456.1:p.Pro1452=
|
|
NM_001351528.1:c.4356A>G
|
NP_001338457.1:p.Pro1452=
|
|
NM_015046.6:c.4356A>G
|
NP_055861.3:p.Pro1452=
|
|
XM_005272172.3:c.4356A>G
|
XP_005272229.1:p.Pro1452=
|
|
XM_005272173.3:c.4356A>G
|
XP_005272230.1:p.Pro1452=
|
|
XM_011518404.3:c.4356A>G
|
XP_011516706.1:p.Pro1452=
|
|
XM_011518405.3:c.4356A>G
|
XP_011516707.1:p.Pro1452=
|
|
XM_011518406.2:c.4356A>G
|
XP_011516708.1:p.Pro1452=
|
|
XM_011518408.3:c.4356A>G
|
XP_011516710.1:p.Pro1452=
|
|
XR_001746251.1:n.4540A>G
|
|
|
XR_929739.2:n.4540A>G
|
|
|
NM_015046.7:c.4356A>G
MANE Select
|
NP_055861.3:p.Pro1452=
|
|
NM_001351528.2:c.4356A>G
|
NP_001338457.1:p.Pro1452=
|
|
NM_001351527.2:c.4356A>G
|
NP_001338456.1:p.Pro1452=
|
|