|
NM_004370.6:c.4300C>T
MANE Select
|
NP_004361.3:p.Arg1434Ter
|
|
ENST00000322507.13:c.4300C>T
MANE Select
|
ENSP00000325146.8:p.Arg1434Ter
|
|
NM_004370.5:c.4300C>T
|
NP_004361.3:p.Arg1434Ter
|
|
NM_080645.2:c.808C>T
|
NP_542376.2:p.Arg270Ter
|
|
NM_080645.3:c.808C>T
|
NP_542376.2:p.Arg270Ter
|
|
ENST00000322507.12:c.4300C>T
|
ENSP00000325146.8:p.Arg1434Ter
|
|
ENST00000345356.10:c.808C>T
|
ENSP00000305147.9:p.Arg270Ter
|
|
ENST00000416123.6:c.4300C>T
|
ENSP00000412864.2:p.Arg1434Ter
|
|
ENST00000419671.1:c.524C>T
|
|
|
ENST00000483888.6:c.4300C>T
|
ENSP00000421216.1:p.Arg1434Ter
|
|
ENST00000615798.4:c.733C>T
|
ENSP00000483232.1:p.Arg245Ter
|
|
XM_011535434.1:c.4300C>T
|
XP_011533736.1:p.Arg1434Ter
|
|
XM_011535435.1:c.4027C>T
|
XP_011533737.1:p.Arg1343Ter
|
|
XM_011535436.1:c.808C>T
|
XP_011533738.1:p.Arg270Ter
|
|
XM_011535436.2:c.808C>T
|
XP_011533738.1:p.Arg270Ter
|
|
XM_017010252.2:c.4264C>T
|
XP_016865741.1:p.Arg1422Ter
|