ENST00000710359.1:c.5789C>T
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ENSP00000518230.1:p.Ala1930Val
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|
ENST00000379802.8:c.7118C>T
MANE Select
|
ENSP00000369129.3:p.Ala2373Val
|
|
ENST00000379802.7:c.7118C>T
|
ENSP00000369129.3:p.Ala2373Val
|
|
ENST00000418664.2:c.5321C>T
|
ENSP00000396591.2:p.Ala1774Val
|
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NM_001008844.1:c.5321C>T
|
NP_001008844.1:p.Ala1774Val
|
|
NM_004415.2:c.7118C>T , LRG_423t1:c.7118C>T
|
NP_004406.2:p.Ala2373Val
|
|
XM_011514323.1:c.5789C>T
|
XP_011512625.1:p.Ala1930Val
|
|
NM_001008844.2:c.5321C>T
|
NP_001008844.1:p.Ala1774Val
|
|
NM_001319034.1:c.5789C>T
|
NP_001305963.1:p.Ala1930Val
|
|
NM_004415.3:c.7118C>T
|
NP_004406.2:p.Ala2373Val
|
|
NM_004415.4:c.7118C>T
MANE Select
|
NP_004406.2:p.Ala2373Val
|
|
NM_001008844.3:c.5321C>T
|
NP_001008844.1:p.Ala1774Val
|
|
NM_001319034.2:c.5789C>T
|
NP_001305963.1:p.Ala1930Val
|
|