ENST00000300658.9:c.*802A>G
MANE Select
|
ENSP00000300658.4:n.*802A>G
|
|
ENST00000300658.8:c.*802A>G
|
ENSP00000300658.4:n.*802A>G
|
|
ENST00000309862.10:n.2150A>G
|
|
|
ENST00000378011.8:c.*802A>G
|
ENSP00000367250.4:n.*802A>G
|
|
ENST00000579146.5:c.*851A>G
|
ENSP00000463234.1:n.*851A>G
|
|
ENST00000614824.4:c.*802A>G
|
ENSP00000480165.1:n.*802A>G
|
|
ENST00000619169.4:c.691A>G
|
ENSP00000478028.1:p.Lys231Glu
|
|
NM_001291726.1:c.*802A>G
|
NP_001278655.1:n.*802A>G
|
|
NM_001291728.1:c.*802A>G
|
NP_001278657.1:n.*802A>G
|
|
NM_001291730.1:c.*802A>G
|
NP_001278659.1:n.*802A>G
|
|
NM_001291732.1:c.*802A>G
|
NP_001278661.1:n.*802A>G
|
|
NM_001291733.1:c.*851A>G
|
NP_001278662.1:n.*851A>G
|
|
NM_033419.4:c.*802A>G
|
NP_219487.3:n.*802A>G
|
|
XM_011525480.2:c.*834A>G
|
XP_011523782.1:n.*834A>G
|
|
XM_011525481.2:c.*802A>G
|
XP_011523783.1:n.*802A>G
|
|
XR_002958086.1:n.2292A>G
|
|
|
NM_033419.5:c.*802A>G
MANE Select
|
NP_219487.3:n.*802A>G
|
|
NM_001291726.2:c.*802A>G
|
NP_001278655.1:n.*802A>G
|
|
NM_001291728.2:c.*802A>G
|
NP_001278657.1:n.*802A>G
|
|
NM_001291730.2:c.*802A>G
|
NP_001278659.1:n.*802A>G
|
|
NM_001291732.2:c.*802A>G
|
NP_001278661.1:n.*802A>G
|
|
NM_001291733.2:c.*851A>G
|
NP_001278662.1:n.*851A>G
|
|