ENST00000480188.2:n.1407G>C
|
|
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ENST00000696279.1:c.4693G>C
|
|
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ENST00000696280.1:n.4462G>C
|
|
|
ENST00000696281.1:c.4391G>C
|
ENSP00000512521.1:p.Gly1464Ala
|
|
ENST00000697921.1:n.3251G>C
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|
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ENST00000697922.1:c.*4363G>C
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ENSP00000513478.1:n.*4363G>C
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|
ENST00000697923.1:n.4818G>C
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|
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ENST00000223642.3:c.4373G>C
MANE Select
|
ENSP00000223642.1:p.Gly1458Ala
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|
ENST00000223642.2:c.4373G>C
|
ENSP00000223642.1:p.Gly1458Ala
|
|
NM_001735.2:c.4373G>C , LRG_28t1:c.4373G>C
|
NP_001726.2:p.Gly1458Ala
|
|
XM_011518980.1:c.4388G>C
|
XP_011517282.1:p.Gly1463Ala
|
|
NM_001317163.1:c.4391G>C
|
NP_001304092.1:p.Gly1464Ala
|
|
NM_001317163.2:c.4391G>C
|
NP_001304092.1:p.Gly1464Ala
|
|
NM_001735.3:c.4373G>C
MANE Select
|
NP_001726.2:p.Gly1458Ala
|
|