ENST00000682565.1:c.7442G>T
|
ENSP00000507671.1:p.Gly2481Val
|
|
ENST00000682801.1:c.7442G>T
|
ENSP00000507862.1:p.Gly2481Val
|
|
ENST00000682859.1:c.7442G>T
|
ENSP00000508222.1:p.Gly2481Val
|
|
ENST00000683791.1:c.834G>T
|
|
|
ENST00000684460.1:c.4894G>T
|
|
|
ENST00000684548.1:c.7442G>T
|
ENSP00000507421.1:p.Gly2481Val
|
|
ENST00000684590.1:c.1889G>T
|
ENSP00000507376.1:p.Gly630Val
|
|
ENST00000684656.1:c.4894G>T
|
|
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ENST00000613296.6:c.7823G>T
MANE Select
|
ENSP00000482968.1:p.Gly2608Val
|
|
ENST00000651434.1:c.896-29993G>T
|
|
|
ENST00000423048.5:c.2654G>T
|
ENSP00000399833.1:p.Gly885Val
|
|
ENST00000484298.5:c.7697G>T
|
ENSP00000478155.1:p.Gly2566Val
|
|
ENST00000613296.4:c.7823G>T
|
ENSP00000482968.1:p.Gly2608Val
|
|
ENST00000614410.4:c.7823G>T
|
ENSP00000479094.1:p.Gly2608Val
|
|
ENST00000620466.4:n.1626G>T
|
|
|
NM_015120.4:c.7826G>T , LRG_741t1:c.7826G>T
|
NP_055935.4:p.Gly2609Val
|
|
NM_001378454.1:c.7823G>T
MANE Select
|
NP_001365383.1:p.Gly2608Val
|
|