ENST00000683572.1:n.775G>T
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ENST00000341947.7:c.4969G>T
MANE Select
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ENSP00000339915.2:p.Gly1657Ter
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ENST00000341947.6:c.4969G>T
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ENSP00000339915.2:p.Gly1657Ter
|
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ENST00000361917.5:c.4648G>T
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ENSP00000355123.1:p.Gly1550Ter
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ENST00000374708.8:c.4711G>T
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ENSP00000363840.4:p.Gly1571Ter
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ENST00000477772.1:n.759G>T
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NM_080679.2:c.4648G>T
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NP_542410.2:p.Gly1550Ter
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NM_080680.2:c.4969G>T
|
NP_542411.2:p.Gly1657Ter
|
|
NM_080681.2:c.4711G>T
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NP_542412.2:p.Gly1571Ter
|
|
XM_011514298.1:c.4123G>T
|
XP_011512600.1:p.Gly1375Ter
|
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XM_011514299.1:c.4255G>T
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XP_011512601.1:p.Gly1419Ter
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XM_011514300.1:c.4075G>T
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XP_011512602.1:p.Gly1359Ter
|
|
XM_011514301.1:c.4012G>T
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XP_011512603.1:p.Gly1338Ter
|
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XM_011514302.1:c.3856G>T
|
XP_011512604.1:p.Gly1286Ter
|
|
XM_011514299.2:c.4255G>T
|
XP_011512601.1:p.Gly1419Ter
|
|
XM_011514300.2:c.4075G>T
|
XP_011512602.1:p.Gly1359Ter
|
|
XM_011514302.2:c.3856G>T
|
XP_011512604.1:p.Gly1286Ter
|
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XM_017010250.1:c.4969G>T
|
XP_016865739.1:p.Gly1657Ter
|
|
XM_017010251.2:c.3787G>T
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XP_016865740.1:p.Gly1263Ter
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|
NM_080680.3:c.4969G>T
MANE Select
|
NP_542411.2:p.Gly1657Ter
|
|
NM_080681.3:c.4711G>T
|
NP_542412.2:p.Gly1571Ter
|
|
NM_080679.3:c.4648G>T
|
NP_542410.2:p.Gly1550Ter
|
|