ENST00000326003.7:c.752A>T
MANE Select
|
ENSP00000314151.1:p.Lys251Met
|
|
ENST00000326003.6:c.752A>T
|
ENSP00000314151.1:p.Lys251Met
|
|
ENST00000360617.7:c.1194A>T
|
ENSP00000353829.2:n.1194A>T
|
|
ENST00000422986.6:c.*408A>T
|
ENSP00000393628.2:n.*408A>T
|
|
ENST00000595392.5:c.*253A>T
|
ENSP00000468912.1:n.*253A>T
|
|
ENST00000595952.5:c.623A>T
|
ENSP00000471155.1:p.Lys208Met
|
|
ENST00000596333.1:n.930A>T
|
|
|
ENST00000598145.1:c.754A>T
|
|
|
ENST00000601349.5:n.2031A>T
|
|
|
ENST00000601812.1:n.1184A>T
|
|
|
ENST00000617027.4:c.629A>T
|
ENSP00000483513.1:p.Lys210Met
|
|
NM_001030047.1:c.*477A>T
|
NP_001025218.1:n.*477A>T
|
|
NM_001030048.1:c.623A>T
|
NP_001025219.1:p.Lys208Met
|
|
NM_001648.2:c.752A>T
MANE Select
|
NP_001639.1:p.Lys251Met
|
|
XM_011526923.1:c.770A>T
|
XP_011525225.1:p.Lys257Met
|
|
XR_935817.1:n.1324+839A>T
|
|
|