ENST00000682114.1:c.211G>T
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ENSP00000507245.1:p.Ala71Ser
|
|
ENST00000682478.1:n.187G>T
|
|
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ENST00000683576.1:n.187G>T
|
|
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ENST00000683627.1:c.211G>T
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ENSP00000507533.1:p.Ala71Ser
|
|
ENST00000684082.1:c.211G>T
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ENSP00000508266.1:p.Ala71Ser
|
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ENST00000684633.1:n.183G>T
|
|
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ENST00000684678.1:c.207G>T
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ENSP00000507059.1:n.207G>T
|
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ENST00000369842.9:c.211G>T
MANE Select
|
ENSP00000358857.4:p.Ala71Ser
|
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ENST00000369835.3:c.106G>T
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ENSP00000358850.3:p.Ala36Ser
|
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ENST00000369842.8:c.211G>T
|
ENSP00000358857.4:p.Ala71Ser
|
|
ENST00000428228.5:c.*116G>T
|
ENSP00000401081.1:n.*116G>T
|
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ENST00000468294.5:n.171G>T
|
|
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ENST00000485261.1:n.187G>T
|
|
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ENST00000486738.5:n.355G>T
|
|
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ENST00000492448.1:n.194G>T
|
|
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ENST00000494443.5:n.268G>T
|
|
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NM_000117.2:c.211G>T , LRG_745t1:c.211G>T
|
NP_000108.1:p.Ala71Ser
|
|
XM_024452349.1:c.3G>T
|
XP_024308117.1:p.Met1Ile
|
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NM_000117.3:c.211G>T
MANE Select
|
NP_000108.1:p.Ala71Ser
|
|