ENST00000254079.9:c.445+513T>G
MANE Select
|
ENSP00000254079.4:n.445+513T>G
|
|
ENST00000254079.8:c.445+513T>G
|
ENSP00000254079.4:n.445+513T>G
|
|
ENST00000394265.5:c.337+513T>G
|
ENSP00000377808.1:n.337+513T>G
|
|
ENST00000394267.2:c.337+513T>G
|
ENSP00000377810.2:n.337+513T>G
|
|
ENST00000492037.5:n.362+513T>G
|
|
|
ENST00000579000.5:c.346+513T>G
|
ENSP00000462841.1:n.346+513T>G
|
|
ENST00000580029.1:n.1949+513T>G
|
|
|
ENST00000580825.5:c.445+513T>G
|
ENSP00000462137.1:n.445+513T>G
|
|
ENST00000583446.5:n.469+513T>G
|
|
|
NM_001242464.1:c.337+513T>G
|
NP_001229393.1:n.337+513T>G
|
|
NM_032192.3:c.445+513T>G
|
NP_115568.2:n.445+513T>G
|
|
NM_181505.3:c.337+513T>G
|
NP_852606.1:n.337+513T>G
|
|
XM_006722137.2:c.445+513T>G
|
XP_006722200.1:n.445+513T>G
|
|
XM_017025216.2:c.445+513T>G
|
XP_016880705.1:n.445+513T>G
|
|
XM_017025217.2:c.337+513T>G
|
XP_016880706.1:n.337+513T>G
|
|
NM_032192.4:c.445+513T>G
MANE Select
|
NP_115568.2:n.445+513T>G
|
|
NM_001242464.2:c.337+513T>G
|
NP_001229393.1:n.337+513T>G
|
|
NM_181505.4:c.337+513T>G
|
NP_852606.1:n.337+513T>G
|
|