ENST00000616432.5:c.*213G>A
MANE Select
|
ENSP00000478908.1:n.*213G>A
|
|
ENST00000406549.7:c.*213G>A
|
ENSP00000383995.3:n.*213G>A
|
|
ENST00000611648.2:c.*213G>A
|
ENSP00000479551.1:n.*213G>A
|
|
ENST00000616432.4:c.*213G>A
|
ENSP00000478908.1:n.*213G>A
|
|
ENST00000618518.3:c.*213G>A
|
ENSP00000481012.1:n.*213G>A
|
|
ENST00000621062.4:c.*213G>A
|
ENSP00000478343.1:n.*213G>A
|
|
NM_001278730.1:c.*213G>A
|
NP_001265659.1:n.*213G>A
|
|
NM_006478.4:c.*213G>A
|
NP_006469.2:n.*213G>A
|
|
NM_152236.2:c.*213G>A
|
NP_689422.1:n.*213G>A
|
|
XM_011529824.1:c.*213G>A
|
XP_011528126.1:n.*213G>A
|
|
XM_011529825.1:c.*213G>A
|
XP_011528127.1:n.*213G>A
|
|
NM_001362985.1:c.*213G>A
|
NP_001349914.1:n.*213G>A
|
|
XM_017028533.1:c.*213G>A
|
XP_016884022.1:n.*213G>A
|
|
NM_001278730.2:c.*213G>A
|
NP_001265659.1:n.*213G>A
|
|
NM_001362985.2:c.*213G>A
|
NP_001349914.1:n.*213G>A
|
|
NM_006478.5:c.*213G>A
|
NP_006469.2:n.*213G>A
|
|
NM_152236.3:c.*213G>A
|
NP_689422.1:n.*213G>A
|
|
NM_001362985.3:c.*213G>A
MANE Select
|
NP_001349914.1:n.*213G>A
|
|
NM_001395196.1:c.*213G>A
|
NP_001382125.1:n.*213G>A
|
|
NM_001395197.1:c.*213G>A
|
NP_001382126.1:n.*213G>A
|
|