ENST00000295754.10:c.1028G=
MANE Select
|
ENSP00000295754.5:p.Ser343=
|
|
ENST00000672866.1:n.2624G=
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|
|
ENST00000295754.9:c.1028G=
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ENSP00000295754.5:p.Ser343=
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|
ENST00000359013.4:c.1103G=
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ENSP00000351905.4:p.Ser368=
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|
NM_001024847.2:c.1103G= , LRG_779t1:c.1103G=
|
NP_001020018.1:p.Ser368=
|
|
NM_003242.5:c.1028G=
|
NP_003233.4:p.Ser343=
|
|
XM_011534043.1:c.1055G=
|
XP_011532345.1:p.Ser352=
|
|
XM_011534044.1:c.980G=
|
XP_011532346.1:p.Ser327=
|
|
XM_011534045.1:c.923G=
|
XP_011532347.1:p.Ser308=
|
|
XM_011534043.2:c.1055G=
|
XP_011532345.1:p.Ser352=
|
|
XM_011534045.3:c.923G=
|
XP_011532347.1:p.Ser308=
|
|
XM_017007106.1:c.923G=
|
XP_016862595.1:p.Ser308=
|
|
NM_003242.6:c.1028G=
MANE Select
|
NP_003233.4:p.Ser343=
|
|