ENST00000454220.7:c.632G>C
|
ENSP00000391905.3:p.Arg211Pro
|
|
ENST00000703395.1:c.-26G>C
|
ENSP00000515286.1:n.-26G>C
|
|
ENST00000703396.1:n.456G>C
|
|
|
ENST00000703397.1:c.-26G>C
|
ENSP00000515287.1:n.-26G>C
|
|
ENST00000703398.1:c.554G>C
|
ENSP00000515288.1:p.Arg185Pro
|
|
ENST00000703421.1:n.665G>C
|
|
|
ENST00000703422.1:c.488G>C
|
ENSP00000515292.1:p.Arg163Pro
|
|
ENST00000703423.1:c.-26G>C
|
ENSP00000515293.1:n.-26G>C
|
|
ENST00000322088.11:c.512G>C
MANE Select
|
ENSP00000324804.6:p.Arg171Pro
|
|
ENST00000322088.10:c.512G>C
|
ENSP00000324804.6:p.Arg171Pro
|
|
ENST00000454220.6:c.632G>C
|
ENSP00000391905.2:p.Arg211Pro
|
|
ENST00000462047.1:n.203G>C
|
|
|
ENST00000462990.5:c.-26G>C
|
ENSP00000470504.1:n.-26G>C
|
|
ENST00000473455.2:n.611G>C
|
|
|
NM_014225.5:c.512G>C
|
NP_055040.2:p.Arg171Pro
|
|
NR_033500.1:n.706G>C
|
|
|
NM_001363656.1:c.-26G>C
|
NP_001350585.1:n.-26G>C
|
|
NM_014225.6:c.512G>C
MANE Select
|
NP_055040.2:p.Arg171Pro
|
|
NM_001363656.2:c.-26G>C
|
NP_001350585.1:n.-26G>C
|
|
NR_033500.2:n.456G>C
|
|
|