ENST00000324071.10:c.1027C>T
MANE Select
|
ENSP00000324648.2:p.Arg343Ter
|
|
ENST00000598834.2:c.1051C>T
|
|
|
ENST00000324071.8:c.1027C>T
|
ENSP00000324648.2:p.Arg343Ter
|
|
ENST00000593831.1:c.319C>T
|
ENSP00000470582.1:p.Arg107Ter
|
|
ENST00000597612.1:n.522C>T
|
|
|
NM_000767.4:c.1027C>T
|
NP_000758.1:p.Arg343Ter
|
|
XM_005258569.3:c.1027C>T
|
XP_005258626.1:p.Arg343Ter
|
|
XM_006723050.2:c.1027C>T
|
XP_006723113.1:p.Arg343Ter
|
|
XM_011526546.1:c.1027C>T
|
XP_011524848.1:p.Arg343Ter
|
|
XM_011526547.1:c.1027C>T
|
XP_011524849.1:p.Arg343Ter
|
|
XM_011526548.1:c.547C>T
|
XP_011524850.1:p.Arg183Ter
|
|
XM_011526549.1:c.436C>T
|
XP_011524851.1:p.Arg146Ter
|
|
XM_011526550.1:c.427C>T
|
XP_011524852.1:p.Arg143Ter
|
|
NM_000767.5:c.1027C>T
MANE Select
|
NP_000758.1:p.Arg343Ter
|
|