ENST00000547103.7:c.6267+150T>G
MANE Select
|
ENSP00000447211.2:n.6267+150T>G
|
|
ENST00000642294.1:c.207+150T>G
|
ENSP00000493572.1:n.207+150T>G
|
|
ENST00000646859.1:c.6132+150T>G
|
ENSP00000496036.1:n.6132+150T>G
|
|
ENST00000298820.7:c.1527+275T>G
|
|
|
ENST00000458043.6:c.6240+150T>G
|
ENSP00000400895.2:n.6240+150T>G
|
|
ENST00000546620.5:n.523+150T>G
|
|
|
ENST00000547103.5:c.6204+150T>G
|
ENSP00000447211.1:n.6204+150T>G
|
|
ENST00000550182.2:c.291+150T>G
|
ENSP00000449641.1:n.291+150T>G
|
|
ENST00000551340.5:c.395+150T>G
|
|
|
NM_173591.3:c.6240+150T>G
|
NP_775862.3:n.6240+150T>G
|
|
XM_005268802.2:c.6291+150T>G
|
XP_005268859.1:n.6291+150T>G
|
|
XM_011538191.1:c.6291+150T>G
|
XP_011536493.1:n.6291+150T>G
|
|
XM_011538192.1:c.6138+150T>G
|
XP_011536494.1:n.6138+150T>G
|
|
XM_011538193.1:c.5925+150T>G
|
XP_011536495.1:n.5925+150T>G
|
|
XM_005268802.3:c.6291+150T>G
|
XP_005268859.1:n.6291+150T>G
|
|
XM_011538192.2:c.6138+150T>G
|
XP_011536494.1:n.6138+150T>G
|
|
NM_001368062.1:c.6105+150T>G
|
NP_001354991.1:n.6105+150T>G
|
|
NM_001368062.3:c.6132+150T>G
|
NP_001354991.2:n.6132+150T>G
|
|
NM_001378609.3:c.6267+150T>G
MANE Select
|
NP_001365538.2:n.6267+150T>G
|
|
NM_001378610.3:c.6267+150T>G
|
NP_001365539.2:n.6267+150T>G
|
|
NM_173591.7:c.6267+150T>G
|
NP_775862.4:n.6267+150T>G
|
|