ENST00000361492.9:c.4621G>T
MANE Select
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ENSP00000354586.5:p.Ala1541Ser
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ENST00000452319.6:c.4672G>T
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ENSP00000390436.1:p.Ala1558Ser
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ENST00000341310.10:c.*3720G>T
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ENSP00000344473.6:n.*3720G>T
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ENST00000361492.8:c.4672G>T
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ENSP00000354586.4:p.Ala1558Ser
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ENST00000438299.5:c.*2544-4G>T
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ENSP00000400593.1:n.*2544-4G>T
|
|
ENST00000445186.5:c.*3771G>T
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ENSP00000397488.1:n.*3771G>T
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ENST00000452319.5:c.4672G>T
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ENSP00000390436.1:p.Ala1558Ser
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ENST00000452692.5:c.*2493-4G>T
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ENSP00000403715.1:n.*2493-4G>T
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NM_005270.4:c.4672G>T
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NP_005261.2:p.Ala1558Ser
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XM_006712422.1:c.4621G>T
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XP_006712485.1:p.Ala1541Ser
|
|
XM_011510969.1:c.4654G>T
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XP_011509271.1:p.Ala1552Ser
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|
XM_011510970.1:c.4531G>T
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XP_011509272.1:p.Ala1511Ser
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|
XM_011510971.1:c.4477G>T
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XP_011509273.1:p.Ala1493Ser
|
|
XM_011510972.1:c.4477G>T
|
XP_011509274.1:p.Ala1493Ser
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|
XM_011510973.1:c.4297G>T
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XP_011509275.1:p.Ala1433Ser
|
|
XM_011510974.1:c.4246G>T
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XP_011509276.1:p.Ala1416Ser
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|
XM_006712422.3:c.4621G>T
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XP_006712485.1:p.Ala1541Ser
|
|
XM_011510969.2:c.4924G>T
|
XP_011509271.2:p.Ala1642Ser
|
|
XM_011510970.2:c.4531G>T
|
XP_011509272.1:p.Ala1511Ser
|
|
XM_011510971.2:c.4477G>T
|
XP_011509273.1:p.Ala1493Ser
|
|
XM_011510972.2:c.4573G>T
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XP_011509274.2:p.Ala1525Ser
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|
XM_011510973.2:c.4297G>T
|
XP_011509275.1:p.Ala1433Ser
|
|
XM_011510974.2:c.4246G>T
|
XP_011509276.1:p.Ala1416Ser
|
|
XM_017003818.1:c.4873G>T
|
XP_016859307.1:p.Ala1625Ser
|
|
XM_024452794.1:c.4672G>T
|
XP_024308562.1:p.Ala1558Ser
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|
XM_024452795.1:c.4672G>T
|
XP_024308563.1:p.Ala1558Ser
|
|
NM_001371271.1:c.4672G>T
|
NP_001358200.1:p.Ala1558Ser
|
|
NM_001374353.1:c.4621G>T
MANE Select
|
NP_001361282.1:p.Ala1541Ser
|
|
NM_001374354.1:c.4246G>T
|
NP_001361283.1:p.Ala1416Ser
|
|
NM_005270.5:c.4672G>T
|
NP_005261.2:p.Ala1558Ser
|
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