ENST00000389048.8:c.3506T>A
MANE Select
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ENSP00000373700.3:p.Leu1169Gln
|
|
ENST00000431873.6:c.733T>A
|
|
|
ENST00000638605.1:n.383T>A
|
|
|
ENST00000642122.1:c.302T>A
|
ENSP00000493203.1:p.Leu101Gln
|
|
ENST00000389048.7:c.3506T>A
|
ENSP00000373700.3:p.Leu1169Gln
|
|
ENST00000431873.5:c.386T>A
|
ENSP00000414027.2:p.Leu129Gln
|
|
ENST00000453137.1:c.200T>A
|
ENSP00000387488.1:p.Leu67Gln
|
|
ENST00000618119.4:c.2375T>A
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ENSP00000482733.1:p.Leu792Gln
|
|
NM_004304.4:c.3506T>A
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NP_004295.2:p.Leu1169Gln
|
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NM_001353765.1:c.302T>A
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NP_001340694.1:p.Leu101Gln
|
|
XM_024452778.1:c.659T>A
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XP_024308546.1:p.Leu220Gln
|
|
XM_024452779.1:c.302T>A
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XP_024308547.1:p.Leu101Gln
|
|
NM_004304.5:c.3506T>A
MANE Select
|
NP_004295.2:p.Leu1169Gln
|
|
NM_001353765.2:c.302T>A
|
NP_001340694.1:p.Leu101Gln
|
|