|
NM_003322.6:c.1199G>A
MANE Select
|
NP_003313.3:p.Arg400Gln
|
|
ENST00000229771.11:c.1199G>A
MANE Select
|
ENSP00000229771.6:p.Arg400Gln
|
|
NM_001289395.1:c.1040G>A
|
NP_001276324.1:p.Arg347Gln
|
|
NM_001289395.2:c.1040G>A
|
NP_001276324.1:p.Arg347Gln
|
|
NM_003322.4:c.1199G>A
|
NP_003313.3:p.Arg400Gln
|
|
NM_003322.5:c.1199G>A
|
NP_003313.3:p.Arg400Gln
|
|
ENST00000229771.10:c.1199G>A
|
ENSP00000229771.6:p.Arg400Gln
|
|
ENST00000322263.8:c.1040G>A
|
ENSP00000319414.4:p.Arg347Gln
|
|
ENST00000373892.4:n.801G>A
|
|
|
ENST00000495781.1:n.375G>A
|
|
|
ENST00000496434.5:n.216G>A
|
|
|
ENST00000614066.4:c.1193G>A
|
ENSP00000477534.1:p.Arg398Gln
|