ENST00000269321.12:c.472T=
MANE Select
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ENSP00000269321.7:p.Phe158=
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ENST00000269321.11:c.472T=
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ENSP00000269321.7:p.Phe158=
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|
ENST00000400721.8:c.416-76T=
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ENSP00000383556.4:n.416-76T=
|
|
ENST00000541078.6:c.472T=
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ENSP00000441348.2:p.Phe158=
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|
ENST00000579121.5:c.472T=
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ENSP00000462960.1:p.Phe158=
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|
ENST00000580033.5:c.*116T=
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ENSP00000463530.1:n.*116T=
|
|
ENST00000580685.5:c.472T=
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ENSP00000464205.1:p.Phe158=
|
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ENST00000581876.5:c.247T=
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ENSP00000461956.1:p.Phe83=
|
|
ENST00000582984.5:n.674T=
|
|
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ENST00000583791.1:n.336T=
|
|
|
ENST00000583868.5:c.435+37T=
|
ENSP00000462209.1:n.435+37T=
|
|
ENST00000584461.5:c.472T=
|
ENSP00000463939.1:p.Phe158=
|
|
NM_001185077.2:c.472T=
|
NP_001172006.1:p.Phe158=
|
|
NM_001185078.2:c.416-76T=
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NP_001172007.1:n.416-76T=
|
|
NM_001301240.1:c.472T=
|
NP_001288169.1:p.Phe158=
|
|
NM_001301241.1:c.472T=
|
NP_001288170.1:p.Phe158=
|
|
NM_001301242.1:c.435+37T=
|
NP_001288171.1:n.435+37T=
|
|
NM_001301243.1:c.607T=
|
NP_001288172.1:p.Phe203=
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|
NM_004309.5:c.472T=
|
NP_004300.1:p.Phe158=
|
|
NR_125441.1:n.531T=
|
|
|
XM_011523574.1:c.607T=
|
XP_011521876.1:p.Phe203=
|
|
NM_004309.6:c.472T=
MANE Select
|
NP_004300.1:p.Phe158=
|
|
NM_001185077.3:c.472T=
|
NP_001172006.1:p.Phe158=
|
|
NM_001185078.3:c.416-76T=
|
NP_001172007.1:n.416-76T=
|
|
NM_001301240.2:c.472T=
|
NP_001288169.1:p.Phe158=
|
|
NM_001301241.2:c.472T=
|
NP_001288170.1:p.Phe158=
|
|
NM_001301242.2:c.435+37T=
|
NP_001288171.1:n.435+37T=
|
|
NM_001301243.2:c.607T=
|
NP_001288172.1:p.Phe203=
|
|
NR_125441.2:n.462T=
|
|
|