ENST00000216361.9:c.1048G>A
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ENSP00000216361.5:p.Ala350Thr
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ENST00000396618.9:c.853G>A
MANE Select
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ENSP00000379862.3:p.Ala285Thr
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ENST00000555117.2:c.910G>A
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ENSP00000493569.1:p.Ala304Thr
|
|
ENST00000643575.1:c.853G>A
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ENSP00000494838.1:p.Ala285Thr
|
|
ENST00000643697.1:n.1155G>A
|
|
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ENST00000644874.2:c.853G>A
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ENSP00000496360.1:p.Ala285Thr
|
|
ENST00000216361.8:c.853G>A
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ENSP00000216361.4:p.Ala285Thr
|
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ENST00000396618.7:c.853G>A
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ENSP00000379862.3:p.Ala285Thr
|
|
ENST00000460581.6:c.517G>A
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ENSP00000451713.1:p.Ala173Thr
|
|
ENST00000468826.2:c.504G>A
|
|
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ENST00000475087.5:c.853G>A
|
ENSP00000451528.1:p.Ala285Thr
|
|
ENST00000555881.5:c.499G>A
|
ENSP00000452569.1:p.Ala167Thr
|
|
ENST00000557065.1:c.635G>A
|
ENSP00000451629.1:n.635G>A
|
|
NM_001135058.1:c.853G>A
|
NP_001128530.1:p.Ala285Thr
|
|
NM_004086.2:c.853G>A
|
NP_004077.1:p.Ala285Thr
|
|
NR_038356.1:n.1352C>T
|
|
|
XM_011536539.1:c.853G>A
|
XP_011534841.1:p.Ala285Thr
|
|
NM_001347720.1:c.1048G>A
|
NP_001334649.1:p.Ala350Thr
|
|
XM_017021071.1:c.1048G>A
|
XP_016876560.1:p.Ala350Thr
|
|
XM_024449506.1:c.910G>A
|
XP_024305274.1:p.Ala304Thr
|
|
NM_004086.3:c.853G>A
MANE Select
|
NP_004077.1:p.Ala285Thr
|
|
NM_001135058.2:c.853G>A
|
NP_001128530.1:p.Ala285Thr
|
|
NM_001347720.2:c.1048G>A
|
NP_001334649.1:p.Ala350Thr
|
|