ENST00000496887.7:c.1173T>G
|
ENSP00000434560.2:p.His391Gln
|
|
ENST00000646564.2:c.990T>G
|
ENSP00000495806.2:p.His330Gln
|
|
ENST00000155840.12:c.1530T>G
MANE Select
|
ENSP00000155840.2:p.His510Gln
|
|
ENST00000335475.6:c.1149T>G
|
ENSP00000334497.5:p.His383Gln
|
|
ENST00000646564.1:c.636T>G
|
ENSP00000495806.1:p.His212Gln
|
|
ENST00000155840.9:c.1530T>G
|
ENSP00000155840.2:p.His510Gln
|
|
ENST00000335475.5:c.1149T>G
|
ENSP00000334497.5:p.His383Gln
|
|
NM_000218.2:c.1530T>G , LRG_287t1:c.1530T>G
|
NP_000209.2:p.His510Gln
|
|
NM_181798.1:c.1149T>G , LRG_287t2:c.1149T>G
|
NP_861463.1:p.His383Gln
|
|
NM_000218.3:c.1530T>G
MANE Select
|
NP_000209.2:p.His510Gln
|
|