ENST00000547103.7:c.6148C>G
MANE Select
|
ENSP00000447211.2:p.Pro2050Ala
|
|
ENST00000642294.1:c.88C>G
|
ENSP00000493572.1:p.Pro30Ala
|
|
ENST00000646859.1:c.6013C>G
|
ENSP00000496036.1:p.Pro2005Ala
|
|
ENST00000298820.7:c.1449C>G
|
|
|
ENST00000458043.6:c.6121C>G
|
ENSP00000400895.2:p.Pro2041Ala
|
|
ENST00000546620.5:n.404C>G
|
|
|
ENST00000547103.5:c.6085C>G
|
ENSP00000447211.1:p.Pro2029Ala
|
|
ENST00000550182.2:c.172C>G
|
ENSP00000449641.1:p.Pro58Ala
|
|
ENST00000551340.5:c.276C>G
|
|
|
NM_173591.3:c.6121C>G
|
NP_775862.3:p.Pro2041Ala
|
|
XM_005268802.2:c.6172C>G
|
XP_005268859.1:p.Pro2058Ala
|
|
XM_011538191.1:c.6172C>G
|
XP_011536493.1:p.Pro2058Ala
|
|
XM_011538192.1:c.6019C>G
|
XP_011536494.1:p.Pro2007Ala
|
|
XM_011538193.1:c.5806C>G
|
XP_011536495.1:p.Pro1936Ala
|
|
XM_005268802.3:c.6172C>G
|
XP_005268859.1:p.Pro2058Ala
|
|
XM_011538192.2:c.6019C>G
|
XP_011536494.1:p.Pro2007Ala
|
|
NM_001368062.1:c.5986C>G
|
NP_001354991.1:p.Pro1996Ala
|
|
NM_001368062.3:c.6013C>G
|
NP_001354991.2:p.Pro2005Ala
|
|
NM_001378609.3:c.6148C>G
MANE Select
|
NP_001365538.2:p.Pro2050Ala
|
|
NM_001378610.3:c.6148C>G
|
NP_001365539.2:p.Pro2050Ala
|
|
NM_173591.7:c.6148C>G
|
NP_775862.4:p.Pro2050Ala
|
|