ENST00000696666.1:n.331G>C
|
|
|
ENST00000704002.1:c.242G>C
|
ENSP00000515615.1:p.Gly81Ala
|
|
ENST00000704003.1:c.*96G>C
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ENSP00000515616.1:n.*96G>C
|
|
ENST00000348035.9:c.143G>C
MANE Select
|
ENSP00000258737.7:p.Gly48Ala
|
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ENST00000348035.8:c.143G>C
|
ENSP00000258737.7:p.Gly48Ala
|
|
ENST00000356142.4:c.143G>C
|
ENSP00000348461.4:p.Gly48Ala
|
|
ENST00000488373.5:n.374G>C
|
|
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ENST00000497741.5:n.159G>C
|
|
|
NM_006908.4:c.143G>C
|
NP_008839.2:p.Gly48Ala
|
|
NM_018890.3:c.143G>C
|
NP_061485.1:p.Gly48Ala
|
|
NM_006908.5:c.143G>C
MANE Select
|
NP_008839.2:p.Gly48Ala
|
|
NM_018890.4:c.143G>C
|
NP_061485.1:p.Gly48Ala
|
|