|
NM_139284.3:c.200T>G
MANE Select
|
NP_644813.1:p.Leu67Arg
|
|
ENST00000310123.8:c.200T>G
MANE Select
|
ENSP00000312273.3:p.Leu67Arg
|
|
NM_139284.2:c.200T>G
|
NP_644813.1:p.Leu67Arg
|
|
ENST00000310123.7:c.200T>G
|
ENSP00000312273.3:p.Leu67Arg
|
|
ENST00000392225.7:c.200T>G
|
ENSP00000376059.3:p.Leu67Arg
|
|
ENST00000473160.6:n.158T>G
|
|
|
ENST00000493050.5:n.259T>G
|
|
|
ENST00000591633.2:c.200T>G
|
ENSP00000467784.1:p.Leu67Arg
|
|
ENST00000591840.5:n.163T>G
|
|
|
ENST00000592346.1:n.148T>G
|
|
|
XM_011526594.1:c.200T>G
|
XP_011524896.1:p.Leu67Arg
|
|
XM_011526595.1:c.-444T>G
|
XP_011524897.1:n.-444T>G
|
|
XM_011526595.2:c.-444T>G
|
XP_011524897.1:n.-444T>G
|
|
XM_017026428.1:c.-317T>G
|
XP_016881917.1:n.-317T>G
|
|
XM_017026429.1:c.-389T>G
|
XP_016881918.1:n.-389T>G
|