ENST00000695666.1:n.849G>C
|
|
|
ENST00000695667.1:n.367G>C
|
|
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ENST00000695668.1:n.2347G>C
|
|
|
ENST00000300692.9:c.362G>C
MANE Select
|
ENSP00000300692.4:p.Gly121Ala
|
|
ENST00000300692.8:c.362G>C
|
ENSP00000300692.4:p.Gly121Ala
|
|
ENST00000392884.2:c.275-325G>C
|
ENSP00000376622.2:n.275-325G>C
|
|
ENST00000526561.1:n.80-325G>C
|
|
|
ENST00000529594.5:c.143G>C
|
ENSP00000437335.1:p.Gly48Ala
|
|
ENST00000534687.5:c.288-325G>C
|
|
|
NM_000732.4:c.362G>C , LRG_37t1:c.362G>C
|
NP_000723.1:p.Gly121Ala
|
|
NM_001040651.1:c.275-325G>C
|
NP_001035741.1:n.275-325G>C
|
|
NM_001040651.2:c.275-325G>C
|
NP_001035741.1:n.275-325G>C
|
|
NM_000732.6:c.362G>C
MANE Select
|
NP_000723.1:p.Gly121Ala
|
|